US11001657B2 - Unbridged indacenyl metallocenes - Google Patents
Unbridged indacenyl metallocenes Download PDFInfo
- Publication number
- US11001657B2 US11001657B2 US16/153,256 US201816153256A US11001657B2 US 11001657 B2 US11001657 B2 US 11001657B2 US 201816153256 A US201816153256 A US 201816153256A US 11001657 B2 US11001657 B2 US 11001657B2
- Authority
- US
- United States
- Prior art keywords
- catalyst
- alkyl
- halogen
- hydrogen
- hydrocarbyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active, expires
Links
- 0 *C(C(*)C1C(*)=C(C(*)(*)C(*)(*)C2([Re])[Re])C2=C(*)C11)C1*=C Chemical compound *C(C(*)C1C(*)=C(C(*)(*)C(*)(*)C2([Re])[Re])C2=C(*)C11)C1*=C 0.000 description 83
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/14—Monomers containing five or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/6592—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
- C08F4/65922—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not
- C08F4/65925—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not two cyclopentadienyl rings being mutually non-bridged
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
- C08F2410/07—Catalyst support treated by an anion, e.g. Cl-, F-, SO42-
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2420/00—Metallocene catalysts
- C08F2420/07—Heteroatom-substituted Cp, i.e. Cp or analog where at least one of the substituent of the Cp or analog ring is or contains a heteroatom
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/02—Low molecular weight, e.g. <100,000 Da.
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/03—Narrow molecular weight distribution, i.e. Mw/Mn < 3
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/06—Comonomer distribution, e.g. normal, reverse or narrow
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65912—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65916—Component covered by group C08F4/64 containing a transition metal-carbon bond supported on a carrier, e.g. silica, MgCl2, polymer
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/6592—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
Definitions
- the present disclosure provides novel unbridged group 4 indacenyl-containing metallocene compound.
- the catalyst system may be used for olefin polymerization processes.
- Polyolefins are widely used commercially because of their robust physical properties. For example, various types of polyethylenes, including high density, low density, and linear low density polyethylenes, are some of the most commercially useful. Polyolefins are typically prepared with a catalyst that polymerizes olefin monomers.
- the present disclosure provides novel unbridged group 4 indacenyl-containing metallocene compounds.
- the novel unbridged group 4 indacenyl-containing metallocene compounds are represented by Formula (I):
- M is a group 4 metal; each of R 1 , R 2 , R 3 , R 4 , and R 8 is independently hydrogen, halogen, C 1 -C 40 hydrocarbyl or C 1 -C 40 substituted hydrocarbyl, —NR′ 2 , —SR′, —OR, —OSiR′ 3 , —PR′ 2 , —R # —SiR′ 3 , where R # is C 1 -C 10 alkyl and each R′ is hydrogen, halogen, C 1 -C 10 alkyl, or C 6 -C 10 aryl; each of R 5 , R 5′ , R 6 , R 6′ , R 7 and R 7′ is independently hydrogen, halogen, C 1 -C 40 hydrocarbyl or C 1 -C 40 substituted hydrocarbyl, —NR′ 2 , —SR′, —OR, —OSiR′ 3 , —PR′ 2 , —R # —SiR′ 3
- the present disclosure also provides a process for polymerization of monomers (such as olefin monomers) comprising contacting one or more monomers with catalyst systems comprising the above catalyst compounds.
- monomers such as olefin monomers
- the present disclosure also provides a process to produce ethylene polymer compositions comprising: i) contacting in a single reaction zone, in the gas phase or slurry phase, ethylene and C 3 to C 20 comonomer with a catalyst system comprising a support, an activator, and one or more catalyst compounds described above, and ii) obtaining an ethylene polymer composition having at least 50 mol % ethylene, preferably having a density of 0.89 g/cc or more (alternately 0.90 g/cc or more, 0.908 g/cc or more, 0.91 g/cc or more, 0.918 g/cc or more, or 0.935 g/cc or more).
- the present disclosure also provides polymer compositions produced by the methods and catalyst systems described herein that preferably have a broad molecular weight distribution for easier processing while maintaining sufficient comonomer incorporation to provide good stiffness and good toughness.
- FIG. 1 is a graph comparing the polydispersity index (Mw/Mn) at various C 6 wt % for polymers prepared with catalysts of the present disclosure with polymers made under the same conditions prepared with comparative catalysts.
- FIG. 2 is a graph comparing the polydispersity index (Mw/Mn) at various C 6 wt % for polymers prepared with catalysts of the present disclosure with polymers made under the same conditions prepared with comparative catalysts.
- FIG. 3 is a graph comparing the comonomer incorporation at various hexene concentrations in the feed for polymers prepared with catalysts of the present disclosure with polymers made under the same conditions prepared with comparative catalysts.
- FIG. 4 is a graph comparing the GPC4D of polymers made by inventive catalysts in Ex. 25, 28, 33, and 50 with polymers made by comparative catalyst in Ex. 57.
- the present disclosure provides novel unbridged group 4 indacenyl-containing metallocene compounds.
- the catalyst systems may be used for olefin polymerization processes.
- Catalyst systems of the present disclosure can provide increased activity or enhanced polymer properties, to increase conversion or comonomer incorporation, or to alter comonomer distribution.
- Catalyst systems and processes of the present disclosure can provide ethylene polymers having the unique properties of high stiffness, high toughness and good processability.
- a “catalyst system” is a combination of one or more catalyst compounds, an activator, and optional support material.
- the catalyst systems may further comprise one or more additional catalyst compounds.
- catalyst systems when catalyst systems are described as comprising neutral stable forms of the components, it is well understood by one of ordinary skill in the art, that the ionic form of the component is the form that reacts with the monomers to produce polymers.
- complex is used to describe molecules in which an ancillary ligand is coordinated to a central transition metal atom.
- the ligand is bulky and stably bonded to the transition metal so as to maintain its influence during use of the catalyst, such as polymerization.
- the ligand may be coordinated to the transition metal by covalent bond and/or electron donation coordination or intermediate bonds.
- the transition metal complexes are generally subjected to activation to perform their polymerization function using an activator which is believed to create a cation as a result of the removal of an anionic group, often referred to as a leaving group, from the transition metal.
- Catalyst precursor is also often referred to as “catalyst precursor,” “pre-catalyst,” “catalyst,” “catalyst compound,” “metal compound,” “metal catalyst compound”, “transition metal compound,” or “transition metal complex.” These words are used interchangeably. “Activator” and “cocatalyst” are also used interchangeably.
- hydrocarbyl radical is defined to be C 1 -C 100 radicals, that may be linear, branched, or cyclic, and when cyclic, aromatic or non-aromatic.
- substituted hydrocarbyl radicals are radicals in which at least one hydrogen atom of the hydrocarbyl radical has been substituted with at least one functional group such as Cl, Br, F, I, NR* 2 , OR*, SeR*, TeR*, PR* 2 , AsR* 2 , SbR* 2 , SR*, BR* 2 , SiR* 3 , GeR* 3 , SnR* 3 , PbR* 3 , and the like (where R* is H or a C 1 to C 20 hydrocarbyl group), or where at least one heteroatom has been inserted within a hydrocarbyl ring.
- R* is H or a C 1 to C 20 hydrocarbyl group
- ring atom means an atom that is part of a cyclic ring structure.
- a benzyl group has six ring atoms and tetrahydrofuran has 5 ring atoms.
- a “ring carbon atom” is a carbon atom that is part of a cyclic ring structure.
- a benzyl group has six ring carbon atoms and para-methylstyrene also has six ring carbon atoms.
- aryl or “aryl group” means a six carbon aromatic ring and the substituted variants thereof, including but not limited to, phenyl, 2-methyl-phenyl, xylyl, 4-bromo-xylyl.
- heteroaryl means an aryl group where a ring carbon atom (or two or three ring carbon atoms) has been replaced with a heteroatom, preferably, N, O, or S.
- a “heterocyclic ring” is a ring having a heteroatom in the ring structure as opposed to a heteroatom substituted ring where a hydrogen on a ring atom is replaced with a heteroatom.
- tetrahydrofuran is a heterocyclic ring and 4-N,N-dimethylamino-phenyl is a heteroatom substituted ring.
- aromatic also refers to pseudoaromatic heterocycles which are heterocyclic substituents that have similar properties and structures (nearly planar) to aromatic heterocyclic ligands, but are not by definition aromatic; likewise, the term aromatic also refers to substituted aromatics.
- continuous means a system that operates without interruption or cessation.
- a continuous process to produce a polymer would be one where the reactants are continually introduced into one or more reactors and polymer product is continually withdrawn.
- an “olefin,” is a linear, branched, or cyclic compound of carbon and hydrogen having at least one double bond.
- olefin is a linear, branched, or cyclic compound of carbon and hydrogen having at least one double bond.
- a copolymer when a copolymer is said to have an “ethylene” content of 35 wt % to 55 wt %, it is understood that the mer unit in the copolymer is derived from ethylene in the polymerization reaction and said derived units are present at 35 wt % to 55 wt %, based upon the weight of the copolymer.
- a “polymer” has two or more of the same or different mer units.
- a “homopolymer” is a polymer having mer units that are the same.
- a “copolymer” is a polymer having two or more mer units that are different from each other.
- “Different” is used to refer to mer units indicates that the mer units differ from each other by at least one atom or are different isomerically. Accordingly, the definition of copolymer, as used herein, includes terpolymers and the like.
- An “ethylene polymer” or “ethylene copolymer” is a polymer or copolymer comprising at least 50 mol % ethylene derived units
- a “propylene polymer” or “propylene copolymer” is a polymer or copolymer comprising at least 50 mol % propylene derived units, and so on.
- an ethylene polymer having a density of 0.86 g/cm 3 or less is referred to as an ethylene elastomer or elastomer; an ethylene polymer having a density of more than 0.86 to less than 0.910 g/cm 3 is referred to as an ethylene plastomer or plastomer; an ethylene polymer having a density of 0.910 to 0.940 g/cm 3 is referred to as a low density polyethylene; and an ethylene polymer having a density of more than 0.940 g/cm 3 is referred to as a high density polyethylene (HDPE).
- HDPE high density polyethylene
- Density is determined according to ASTM D 1505 using a density-gradient column on a compression-molded specimen that has been slowly cooled to room temperature (i.e., over a period of 10 minutes or more) and allowed to age for a sufficient time that the density is constant within +/ ⁇ 0.001 g/cm 3 ).
- Linear low density polyethylene (LLDPE) and has been produced with conventional Ziegler-Natta catalysts, vanadium catalysts, or with metallocene catalysts in gas phase reactors and/or in slurry reactors and/or in solution reactors.
- Linear means that the polyethylene has no long chain branches, typically referred to as a branching index (g′ vis ) of 0.97 or above, preferably 0.98 or above. Branching index, g′ vis , is measured by GPC-4D as described below.
- ethylene shall be considered an ⁇ -olefin.
- M n is number average molecular weight
- M w is weight average molecular weight
- M z is z average molecular weight
- wt % is weight percent
- mol % is mole percent.
- Mw, Mn, Mz Molecular weight distribution
- PDI polydispersity index
- room temperature is approx. 23° C.
- Me is methyl
- Et is ethyl
- t-Bu and t Bu are tertiary butyl
- iPr and i Pr are isopropyl
- Cy is cyclohexyl
- THF also referred to as thf
- Bn is benzyl
- Ph is phenyl
- Cp is cyclopentadienyl
- Cp* is pentamethyl cyclopentadienyl
- Ind is indenyl
- Flu is fluorenyl
- MAO is methylalumoxane.
- M is a group 4 metal, preferably HF, Zr or Ti, preferably Hf or Zr; each of R 1 , R 2 , R 3 , R 4 , and R 8 is independently hydrogen, halogen, C 1 -C 40 hydrocarbyl or C 1 -C 40 substituted hydrocarbyl, —NR′ 2 , —SR′, —OR, —OSiR′ 3 , —PR′ 2 , —R # —SiR′ 3 , where R # is C 1 -C 10 alkyl and each R′ is hydrogen, halogen, C 1 -C 10 alkyl, or C 6 -C 10 aryl; each of R 5 , R 5′ , R 6 , R 6′ , R 7 , and R 7′ is independently hydrogen, halogen, C 1 -C 40 hydrocarbyl or C 1 -C 40 substituted hydrocarbyl, —NR′ 2 , —SR′, —OR, —OSiR′ 3
- each of R 1 , R 2 , R 3 , and R 4 is independently halogen, C 1 -C 40 hydrocarbyl or C 1 -C 40 substituted hydrocarbyl, —NR′ 2 , —SR′, —OR, —OSiR′ 3 , —PR′ 2 , —R # —SiR′ 3 , where R # is C 1 -C 10 alkyl and each R′ is hydrogen, halogen, C 1 -C 10 alkyl, or C 6 -C 10 aryl.
- R 2 and R 3 can be hydrogen
- one of the R 1 and R 4 can be hydrogen
- R 2 , R 3 and at least one of R 1 and R 4 are hydrogen.
- the present disclosure further provides a process for polymerization of olefin monomers comprises contacting one or more monomers with catalyst systems comprising activator, one or more catalyst compounds represented by the Formula I and a support.
- the present disclosure provides a process to produce ethylene polymer compositions comprising: contacting in a single reaction zone, in the gas phase or slurry phase, ethylene and C 3 to C 20 comonomer with a catalyst system comprising a support, an activator, and one or more catalyst compounds described above, and obtaining an olefin polymer (such as ethylene homo- or co-polymer).
- novel catalyst compounds of the present disclosure are represented by Formula (I):
- M is a group 4 metal, preferably Hf or Zr; each of R 1 , R 2 , R 3 , R 4 , and R 8 is independently hydrogen, halogen, C 1 -C 40 hydrocarbyl or C 1 -C 40 substituted hydrocarbyl, —NR′ 2 , —SR′, —OR, —OSiR′ 3 , —PR′ 2 , —R # —SiR′ 3 , where R # is C 1 -C 10 alkyl (preferably C 1 to C 10 alpha olefin, preferably, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, or an isomer thereof) and each R′ is hydrogen, halogen, C 1 -C 10 alkyl, or C 6 -C 10 aryl (preferably each of R 1 , R 2 , R 3 , R 4
- R 4 , R 8 , R 5 , R 5′ , R 6 , R 6′ , R 7 , and R 7′ are as defined above.
- M is a group 4 metal (such as Zr or Hf); each of R 1 , R 2 , R 3 , R 4 , and R 5 is independently hydrogen, halogen, C 1 -C 20 substituted or unsubstituted hydrocarbyl, halocarbyl or silylcarbyl; each of R 5 , R 5′ , R 6 , R 6′ , R 7 , and R 7′ is independently hydrogen or a C 1 -C 10 alkyl; each X is independently a leaving group, or two Xs are joined and bound to the metal atom to form a metallocycle ring, or two Xs are joined to form a chelating ligand, a diene, or an alkylidene; and each of R 9 , R 10 , R 11 , R 12 , and R 13 is hydrogen or C 1 -C 20 substituted or unsubstituted hydrocarbyl, or R 9 and R 10 or R 12 and R 13 together form a
- R 2 is hydrogen or a C 1 to C 12 alkyl group, such as methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof.
- R 9 and R 10 together form an unsaturated cyclic ring structure.
- the unsaturated cyclic ring may be substituted with bromo or phenyl which may be substituted or unsubstituted.
- each of R 5 , R 5′ , R 6 , R 6′ , R 7 , and R 7′ is independently is H, or methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof).
- each of R 5 , R 5′ , R 6 , R 6′ , R 7 , and R 7′ is H, alternately R 5 , R 5′ , R 7 , and R 7′ are H, and R 6 and R 6′ are independently, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof.
- R 12 is C 1 -C 20 unsubstituted hydrocarbyl, preferably butyl.
- each X may be, independently, a halide, a hydride, an alkyl group, an alkenyl group or an arylalkyl group.
- R 4 is —R # —SiR′ 3 , where R # is C 1 -C 10 alkyl (preferably, C 1 to C 10 alpha olefin, preferably, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, or an isomer thereof) and R′ is, halogen, C 1 -C 10 alkyl or C 6 -C 10 aryl, preferably, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, phenyl or an isomer thereof), preferably R 4 is CH 2 SiMe 3 .
- R 12 is —R # —SiR′ 3 , where R # is C 1 -C 10 alkyl (preferably, C 1 to C 10 alpha olefin, preferably, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, or an isomer thereof) and R′ is, halogen, C 1 -C 10 alkyl or C 6 -C 10 aryl, preferably, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, phenyl or an isomer thereof), preferably R 12 is CH 2 SiMe 3 .
- each X is independently selected from the group consisting of hydrocarbyl radicals having from 1 to 20 carbon atoms, aryls, hydrides, amides, alkoxides, sulfides, phosphides, halides, dienes, amines, phosphines, ethers, and a combination thereof, (two Xs may form a part of a fused ring or a ring system), preferably each X is independently selected from halides, aryls and C 1 to C 5 alkyl groups, preferably each X is a phenyl, methyl, ethyl, propyl, butyl, pentyl, bromo, or chloro group.
- M is a group 4 metal
- each of R 1 , R 2 , R 3 , R 4 , and R 8 is independently hydrogen, halogen, C 1 -C 20 substituted or unsubstituted hydrocarbyl, halocarbyl or silylcarbyl;
- each of R 5 , R 5′ , R 6 , R 6′ , R 7 , and R 7′ is independently hydrogen or a C 1 -C 10 alkyl
- each X is independently a leaving group, or two Xs are joined and bound to the metal atom to form a metallocycle ring, or two Xs are joined to form a chelating ligand, a diene, or an alkylidene;
- each of R 9 , R 10 , R 11 , R 12 , and R 13 is hydrogen or C 1 -C 20 substituted or unsubstituted hydrocarbyl, or R 9 and R 10 or R 12 and R 13 together form a substituted or unsubstituted 5-8 membered saturated or unsaturated cyclic ring.
- R 9 and R 10 together form an unsaturated cyclic ring structure, preferably the unsaturated cyclic ring is substituted with bromo or phenyl which may be substituted or unsubstituted.
- R 4 is selected from aryl, alkyl, bromo, chloro, or fluoro.
- R 12 is C 1 -C 20 unsubstituted hydrocarbyl, preferably R 12 is butyl.
- R 2 is C 1 -C 20 unsubstituted hydrocarbyl, preferably R 2 is methyl.
- R 2 is hydrogen
- Useful asymmetric catalysts are preferably such that a mirror plane cannot be drawn through the metal center and the cyclopentadienyl moieties bridged to the metal center are structurally different.
- Catalyst compounds useful herein are represented by one or more of:
- Catalyst compounds useful herein are represented by one or more of:
- Preferred catalyst compounds useful herein are represented by Formula (II):
- each of R 1 , R 2 , R 3 , and R 4 is independently halogen, C 1 -C 40 hydrocarbyl or C 1 -C 40 substituted hydrocarbyl, —NR′ 2 , —SR′, —OR, —OSiR′ 3 , —PR′ 2 , where each R′ is hydrogen, halogen, C 1 -C 10 alkyl, or C 6 -C 10 aryl (preferably each of R 1 , R 2 , R 3 , and R 4 , is independently H, C 6 -C 10 aryl, or a C 1 to C 40 alpha olefin, preferably, C 6 -C 10 aryl, or C 2 to C 20 alpha olefin, preferably, C 6 -C 10 aryl, or C 2 to C 12 alpha olefin, preferably, phenyl, naphthyl, methyl, ethyl, propyl, butyl, pentyl, preferably,
- R 2 and R 3 can be hydrogen, one of the R 1 and R 4 can be hydrogen, or R 2 , R 3 and at least one of R 1 and R 4 are hydrogen.
- R 1 is substituted or unsubstituted aryl or halogen, such as substituted or unsubstituted phenyl, chloro, idodo, or bromo.
- R 4 is substituted or unsubstituted aryl or halogen, such as substituted or unsubstituted phenyl, chloro, idodo, or bromo.
- R 1 and R 4 are, independently, substituted or unsubstituted aryl or halogen, such as substituted or unsubstituted phenyl, chloro, idodo or bromo.
- R 2 is H, phenyl, naphthyl, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof.
- R 3 is H, phenyl, naphthyl, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof.
- R 2 and R 3 are, independently, H, phenyl, naphthyl, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof.
- R 1 and R 4 are, independently, substituted or unsubstituted aryl or halogen, such as substituted or unsubstituted phenyl, chloro, idodo, or bromo
- R 2 and R 3 are, independently, H, phenyl, naphthyl, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof.
- Catalyst compounds useful herein include one or more of those represented by the formula:
- the catalyst systems can comprise a support material.
- the support material is a porous support material, for example, talc, and inorganic oxides.
- Other support materials include zeolites, clays, organoclays, or any other organic or inorganic support material, or mixtures thereof.
- support and “support material” are used interchangeably.
- the support material is an inorganic oxide in a finely divided form.
- Suitable inorganic oxide materials for use in the supported catalyst systems herein include Groups 2, 4, 13, and 14 metal oxides such as silica, alumina, and mixtures thereof.
- Other inorganic oxides that may be employed, either alone or in combination, with the silica or alumina are magnesia, titania, zirconia, and the like.
- Other suitable support materials can be employed, for example, finely divided functionalized polyolefins such as finely divided polyethylene.
- Particularly useful supports include magnesia, titania, zirconia, montmorillonite, phyllosilicate, zeolites, talc, clays, and the like.
- support materials may be used, for example, silica-chromium, silica-alumina, silica-titania, and the like.
- Preferred support materials include Al 2 O 3 , ZrO 2 , SiO 2 , and combinations thereof, more preferably, SiO 2 , Al 2 O 3 , or SiO 2 /Al 2 O 3 .
- the support material most preferably, an inorganic oxide, has a surface area in the range of from about 10 m 2 /g to about 700 m 2 /g, pore volume in the range of from about 0.1 cc/g to about 4.0 cc/g, and average particle size in the range of from about 5 m to about 500 m. More preferably, the surface area of the support material is in the range of from about 50 m 2 /g to about 500 m 2 /g, pore volume of from about 0.5 cc/g to about 3.5 cc/g, and average particle size of from about 10 m to about 200 m.
- the surface area of the support material is in the range of from about 100 m 2 /g to about 400 m 2 /g, pore volume from about 0.8 cc/g to about 3.0 cc/g, and average particle size is from about 5 m to about 100 ⁇ m.
- the average pore size of the support material can be from 10 to 1,000 ⁇ , preferably, 50 to about 500 ⁇ , and most preferably, 75 to about 350 ⁇ .
- the support material is a high surface area, amorphous silica (surface area ⁇ 300 m 2 /gm, pore volume ⁇ 1.65 cm 3 /gm), and is marketed under the tradenames of DAVISON 952 or DAVISON 955 by the Davison Chemical Division of W. R. Grace and Company, are particularly useful. In other embodiments, DAVIDSON 948 is used.
- the support material may be dry, that is, free of absorbed water. Drying of the support material can be achieved by heating or calcining at about 100° C. to about 1000° C., preferably, at least about 600° C.
- the support material is silica, it is typically heated to at least 200° C., preferably, about 200° C. to about 850° C., and most preferably, at about 600° C.; and for a time of about 1 minute to about 100 hours, from about 12 hours to about 72 hours, or from about 24 hours to about 60 hours.
- the calcined support material preferably, has at least some reactive hydroxyl (OH) groups.
- the support material is fluorided.
- Fluoriding agent containing compounds may be any compound containing a fluorine atom.
- Particularly desirable are inorganic fluorine containing compounds are selected from the group consisting of NH 4 BF 4 , (NH 4 ) 2 SiF 6 , NH 4 PF 6 , NH 4 F, (NH 4 ) 2 TaF 7 , NH 4 NbF 4 , (NH 4 ) 2 GeF 6 , (NH 4 ) 2 SmF 6 , (NH 4 ) 2 TiF 6 , (NH 4 ) 2 ZrF 6 , MoF 6 , ReF 6 , GaF 3 , SO 2 ClF, F 2 , SiF 4 , SF 6 , ClF 3 , CkF 5 , BrF 5 , IF 7 , NF 3 , HF, BF 3 , NHF 2 , and NH 4 HF 2 .
- Ammonium hexafluorosilicate and ammonium tetrafluoroborate fluorine compounds are typically solid particulates as are the silicon dioxide supports.
- a desirable method of treating the support with the fluorine compound is to dry mix the two components by blending at a concentration of from 0.01 to 10.0 millimole F/g of support, desirably in the range of from 0.05 to 6.0 millimole F/g of support, and most desirably in the range of from 0.1 to 3.0 millimole F/g of support.
- the fluorine compound can be dry mixed with the support either before or after charging to a vessel for dehydration or calcining the support.
- the fluorine concentration present on the support is in the range of from 0.1 to 25 wt %, alternatively from 0.19 to 19 wt %, alternatively from 0.6 to 3.5 wt %, based upon the weight of the support.
- the above two metal catalyst components described herein are generally deposited on the support material at a loading level of 10-100 micromoles of metal per gram of solid support; alternatively 20-80 micromoles of metal per gram of solid support; or 40-60 micromoles of metal per gram of support. But greater or lesser values may be used provided that the total amount of solid complex does not exceed the support's pore volume.
- the support material comprises a support material treated with an electron-withdrawing anion.
- the support material can be silica, alumina, silica-alumina, silica-zirconia, alumina-zirconia, aluminum phosphate, heteropolytungstates, titania, magnesia, boria, zinc oxide, mixed oxides thereof, or mixtures thereof; and the electron-withdrawing anion is selected from fluoride, chloride, bromide, phosphate, triflate, bisulfate, sulfate, or any combination thereof.
- the electron-withdrawing component used to treat the support material can be any component that increases the Lewis or Br ⁇ nsted acidity of the support material upon treatment (as compared to the support material that is not treated with at least one electron-withdrawing anion).
- the electron-withdrawing component is an electron-withdrawing anion derived from a salt, an acid, or other compound, such as a volatile organic compound, that serves as a source or precursor for that anion.
- Electron-withdrawing anions can be sulfate, bisulfate, fluoride, chloride, bromide, iodide, fluorosulfate, fluoroborate, phosphate, fluorophosphate, trifluoroacetate, triflate, fluorozirconate, fluorotitanate, phospho-tungstate, or mixtures thereof, or combinations thereof.
- An electron-withdrawing anion can be fluoride, chloride, bromide, phosphate, triflate, bisulfate, or sulfate, and the like, or any combination thereof, at least one embodiment of this disclosure.
- the electron-withdrawing anion is sulfate, bisulfate, fluoride, chloride, bromide, iodide, fluorosulfate, fluoroborate, phosphate, fluorophosphate, trifluoroacetate, triflate, fluorozirconate, fluorotitanate, or combinations thereof.
- the support material suitable for use in the catalyst systems of the present disclosure can be one or more of fluorided alumina, chlorided alumina, bromided alumina, sulfated alumina, fluorided silica-alumina, chlorided silica-alumina, bromided silica-alumina, sulfated silica-alumina, fluorided silica-zirconia, chlorided silica-zirconia, bromided silica-zirconia, sulfated silica-zirconia, fluorided silica-titania, fluorided silica-coated alumina, sulfated silica-coated alumina, phosphated silica-coated alumina, and the like, or combinations thereof.
- the activator-support can be, or can comprise, fluorided alumina, sulfated alumina, fluorided silica-alumina, sulfated silica-alumina, fluorided silica-coated alumina, sulfated silica-coated alumina, phosphated silica-coated alumina, or combinations thereof.
- the support material includes alumina treated with hexafluorotitanic acid, silica-coated alumina treated with hexafluorotitanic acid, silica-alumina treated with hexafluorozirconic acid, silica-alumina treated with trifluoroacetic acid, fluorided boria-alumina, silica treated with tetrafluoroboric acid, alumina treated with tetrafluoroboric acid, alumina treated with hexafluorophosphoric acid, or combinations thereof.
- any of these activator-supports optionally can be treated with a metal ion.
- Nonlimiting examples of cations suitable for use in the present disclosure in the salt of the electron-withdrawing anion include ammonium, trialkyl ammonium, tetraalkyl ammonium, tetraalkyl phosphonium, H+, [H(OEt 2 ) 2 ]+, or combinations thereof.
- combinations of one or more different electron-withdrawing anions can be used to tailor the specific acidity of the support material to a desired level.
- Combinations of electron-withdrawing components can be contacted with the support material simultaneously or individually, and in any order that provides a desired chemically-treated support material acidity.
- two or more electron-withdrawing anion source compounds in two or more separate contacting steps.
- one example of a process by which a chemically-treated support material is prepared is as follows: a selected support material, or combination of support materials, can be contacted with a first electron-withdrawing anion source compound to form a first mixture; such first mixture can be calcined and then contacted with a second electron-withdrawing anion source compound to form a second mixture; the second mixture can then be calcined to form a treated support material.
- the first and second electron-withdrawing anion source compounds can be either the same or different compounds.
- the method by which the oxide is contacted with the electron-withdrawing component can include, but is not limited to, gelling, co-gelling, impregnation of one compound onto another, and the like, or combinations thereof.
- the contacted mixture of the support material, electron-withdrawing anion, and optional metal ion can be calcined.
- the support material can be treated by a process comprising: (i) contacting a support material with a first electron-withdrawing anion source compound to form a first mixture; (ii) calcining the first mixture to produce a calcined first mixture; (iii) contacting the calcined first mixture with a second electron-withdrawing anion source compound to form a second mixture; and (iv) calcining the second mixture to form the treated support material.
- the catalyst systems may be formed by combining the above metal catalyst components with activators in any manner known from the literature including by supporting them for use in slurry or gas phase polymerization.
- Activators are defined to be any compound which can activate any one of the catalysts described above by converting the neutral metal compound to a catalytically active metal compound cation.
- Non-limiting activators include alumoxanes, aluminum alkyls, ionizing activators, which may be neutral or ionic, and conventional-type cocatalysts.
- Preferred activators typically include alumoxane compounds, modified alumoxane compounds, and ionizing anion precursor compounds that abstract a reactive, G-bound, metal ligand making the metal compound cationic and providing a charge-balancing noncoordinating or weakly coordinating anion.
- Alumoxane activators are utilized as activators in the catalyst systems described herein.
- Alumoxanes are generally oligomeric compounds containing —Al(R 1 )—O— sub-units, where R 1 is an alkyl group.
- Examples of alumoxanes include methylalumoxane (MAO), modified methylalumoxane (MMAO), ethylalumoxane and isobutylalumoxane.
- Alkylalumoxanes and modified alkylalumoxanes are suitable as catalyst activators, particularly when the abstractable ligand is an alkyl, halide, alkoxide, or amide.
- alumoxanes Mixtures of different alumoxanes and modified alumoxanes may also be used. It may be preferable to use a visually clear methylalumoxane.
- a cloudy or gelled alumoxane can be filtered to produce a clear solution or clear alumoxane can be decanted from the cloudy solution.
- a useful alumoxane is a modified methyl alumoxane (MMAO) cocatalyst type 3A (commercially available from Akzo Chemicals, Inc. under the trade name Modified Methylalumoxane type 3A, covered under patent number U.S. Pat. No. 5,041,584).
- MMAO modified methyl alumoxane
- the activator is an alumoxane (modified or unmodified)
- some embodiments select the maximum amount of activator typically at up to a 5000-fold molar excess Al/M over the catalyst (per metal catalytic site).
- the minimum activator-to-catalyst-compound is a 1:1 molar ratio. Alternate preferred ranges include from 1:1 to 500:1, alternatively from 1:1 to 200:1, alternatively from 1:1 to 100:1, or alternatively from 1:1 to 50:1.
- alumoxane is present at zero mol %, alternatively the alumoxane is present at a molar ratio of aluminum to catalyst compound transition metal less than 500:1, preferably less than 300:1, preferably less than 100:1, preferably less than 1:1.
- non-coordinating anion means an anion which either does not coordinate to a cation or which is only weakly coordinated to a cation thereby remaining sufficiently labile to be displaced by a neutral Lewis base.
- “Compatible” non-coordinating anions are those which are not degraded to neutrality when the initially formed complex decomposes. Further, the anion will not transfer an anionic substituent or fragment to the cation so as to cause it to form a neutral transition metal compound and a neutral by-product from the anion.
- Non-coordinating anions useful in accordance with embodiments of the present disclosure are those that are compatible, stabilize the transition metal cation in the sense of balancing its ionic charge at +1, and yet retain sufficient lability to permit displacement during polymerization.
- an ionizing activator such as tri (n-butyl) ammonium tetrakis (pentafluorophenyl) borate, a tris perfluorophenyl boron metalloid precursor or a tris perfluoronaphthyl boron metalloid precursor, polyhalogenated heteroborane anions (WO 98/43983), boric acid (U.S. Pat. No. 5,942,459), or combination thereof. It is also within the scope of the present disclosure to use neutral or ionic activators alone or in combination with alumoxane or modified alumoxane activators.
- Preferred activators include N,N-dimethylanilinium tetrakis(perfluoronaphthyl)borate, N,N-dimethylanilinium tetrakis(perfluorobiphenyl)borate, N,N-dimethylanilinium tetrakis(perfluorophenyl)borate, N,N-dimethylanilinium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate, triphenylcarbenium tetrakis(perfluoronaphthyl)borate, triphenylcarbenium tetrakis(perfluorobiphenyl)borate, triphenylcarbenium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate, triphenylcarbenium tetrakis(perfluorophenyl)borate, [Me 3 NH + ][B(C 6 F 5
- the activator comprises a triaryl carbonium (such as triphenylcarbenium tetraphenylborate, triphenylcarbenium tetrakis(pentafluorophenyl)borate, triphenylcarbenium tetrakis-(2,3,4,6-tetrafluorophenyl)borate, triphenylcarbenium tetrakis(perfluoronaphthyl)borate, triphenylcarbenium tetrakis(perfluorobiphenyl)borate, triphenylcarbenium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate).
- a triaryl carbonium such as triphenylcarbenium tetraphenylborate, triphenylcarbenium tetrakis(pentafluorophenyl)borate, triphenylcarbenium tetrakis-(2,3,4,6-tetra
- the activator comprises one or more of trialkylammonium tetrakis(pentafluorophenyl)borate, N,N-dialkylanilinium tetrakis(pentafluorophenyl)borate, N,N-dimethyl-(2,4,6-trimethylanilinium) tetrakis(pentafluorophenyl)borate, trialkylammonium tetrakis-(2,3,4,6-tetrafluorophenyl) borate, N,N-dialkylanilinium tetrakis-(2,3,4,6-tetrafluorophenyl)borate, trialkylammonium tetrakis(perfluoronaphthyl)borate, N,N-dialkylanilinium tetrakis(perfluoronaphthyl)borate, trialkylammonium tetrakis(perfluorobiphenyl)borate,
- the typical activator-to-catalyst ratio e.g., all NCA activators-to-catalyst ratio is about a 1:1 molar ratio.
- Alternate preferred ranges include from 0.1:1 to 100:1, alternatively from 0.5:1 to 200:1, alternatively from 1:1 to 500:1 alternatively from 1:1 to 1000:1.
- a particularly useful range is from 0.5:1 to 10:1, preferably 1:1 to 5:1.
- Aluminum alkyl or organoaluminum compounds which may be utilized as co-activators include, for example, trimethylaluminum, triethylaluminum, triisobutylaluminum, tri-n-hexylaluminum, tri-n-octylaluminum, and diethyl zinc.
- the catalyst systems will additionally comprise one or more scavenging compounds.
- the term “scavenger” means a compound that removes polar impurities from the reaction environment. These impurities adversely affect catalyst activity and stability.
- the scavenging compound will be an organometallic compound such as the Group-13 organometallic compounds of U.S. Pat. Nos. 5,153,157; 5,241,025; and WO 91/09882; WO 94/03506; WO 93/14132; and that of WO 95/07941.
- Exemplary compounds include triethyl aluminum, triethyl borane, tri-iso-butyl aluminum, methyl alumoxane, iso-butyl alumoxane, and tri-n-octyl aluminum.
- Those scavenging compounds having bulky or C 6 -C 20 linear hydrocarbyl substituents connected to the metal or metalloid center usually minimize adverse interaction with the active catalyst.
- Examples include triethyl aluminum, but more preferably, bulky compounds such as tri-iso-butyl aluminum, tri-iso-prenyl aluminum, and long-chain linear alkyl-substituted aluminum compounds, such as tri-n-hexyl aluminum, tri-n-octyl aluminum, or tri-n-dodecyl aluminum.
- bulky compounds such as tri-iso-butyl aluminum, tri-iso-prenyl aluminum, and long-chain linear alkyl-substituted aluminum compounds, such as tri-n-hexyl aluminum, tri-n-octyl aluminum, or tri-n-dodecyl aluminum.
- Preferred aluminum scavengers include those where there is oxygen present. That is, the material per se or the aluminum mixture used as a scavenger, includes an aluminum/oxygen species, such as an alumoxane or alkylaluminum oxides, e.g., dialkyaluminum oxides, such as bis(diisobutylaluminum) oxide.
- aluminum containing scavengers can be represented by the formula ((R z —Al—) y O—) x , wherein z is 1-2, y is 1-2, x is 1-100, and R is a C 1 -C 12 hydrocarbyl group.
- the scavenger has an oxygen to aluminum (O/Al) molar ratio of from about 0.25 to about 1.5, more particularly from about 0.5 to about 1.
- the above catalyst compounds can be combined to form a catalyst system.
- One or more (such as two or more) metal catalyst compounds can be added together in a desired ratio when combined, contacted with an activator, or contacted with a support material or a supported activator.
- the metal catalyst compounds may be added to the mixture sequentially or at the same time.
- Alternative preparations can include addition of a first metal catalyst compound to a slurry including a support or a supported activator mixture for a specified reaction time, followed by the addition of the second metal catalyst compound solution, mixed for another specified time, after which the mixture may be recovered for use in a polymerization reactor, such as by spray drying.
- another additive such as 1-hexene in about 10 vol % can be present in the mixture prior to the addition of the metal catalyst compound.
- the catalyst compound may be supported via contact with a support material for a reaction time.
- the resulting supported catalyst composition may then be mixed with diluent to form a slurry, which may or may not include an activator.
- the slurry may then be optionally admixed with a second metal catalyst compound prior to introduction of the resulting mixed catalyst system to a polymerization reactor.
- the second metal catalyst compound may be admixed at any point prior to introduction to the reactor, such as in a polymerization feed vessel or in-line in a catalyst delivery system.
- the catalyst system may be formed by combining the catalyst compound with a support and an activator, desirably in a first diluent such as an alkane or toluene, to produce a supported, activated catalyst compound.
- a first diluent such as an alkane or toluene
- the supported activated catalyst compound is then combined in one embodiment with a high viscosity diluent such as mineral or silicon oil, or an alkane diluent comprising from 5 to 99 wt % mineral or silicon oil to form a slurry of the supported metal catalyst compound, followed by, or simultaneous to combining with an optional second metal catalyst compound (for example, a metal catalyst compound useful for producing a second polymer attribute, such as a low molecular weight polymer fraction or low comonomer content), either in a diluent or as the dry solid compound, to form a supported activated mixed catalyst system.
- the diluent consists of mineral oil.
- Mineral oil or “high viscosity diluents,” as used herein refers to petroleum hydrocarbons and mixtures of hydrocarbons that may include aliphatic, aromatic, and/or paraffinic components that are liquids at 23° C. and above, and typically have a molecular weight of at least 300 amu to 500 amu or more, and a viscosity at 40° C. of from 40 to 300 cSt or greater, or from 50 to 200 cSt in a particular embodiment.
- mineral oil includes synthetic oils or liquid polymers, polybutenes, refined naphthenic hydrocarbons, and refined paraffins known in the art, such as disclosed in BLUE BOOK 2001, MATERIALS, COMPOUNDING INGREDIENTS, MACHINERY AND SERVICES FOR RUBBER 189 247 (J. H. Lippincott, D. R. Smith, K. Kish & B. Gordon eds. Lippincott & Peto Inc. 2001).
- Preferred mineral and silicon oils are those that exclude moieties that are reactive with metallocene catalysts, examples of which include hydroxyl and carboxyl groups.
- the diluent may comprise a blend of a mineral, silicon oil, and/or and a hydrocarbon selected from the group consisting of C 1 to C 10 alkanes, C 6 to C 20 aromatic hydrocarbons, C 7 to C 21 alkyl-substituted hydrocarbons, and mixtures thereof.
- the diluent may comprise from 5 to 99 wt % mineral oil.
- the diluent may consist essentially of mineral oil.
- the catalyst compound is combined with an activator and a first diluent to form a catalyst slurry that is then combined with a support material.
- the support particles are preferably not previously activated.
- the catalyst compound can be in any desirable form such as a dry powder, suspension in a diluent, solution in a diluent, liquid, etc.
- the catalyst slurry and support particles are then mixed thoroughly, in one embodiment at an elevated temperature, so that both the catalyst compound and the activator are deposited on the support particles to form a support slurry.
- a wide range of mixing temperatures may be used at various stages of making the catalyst system.
- the mixture is preferably, heated to a first temperature of from 25° C. to 150° C., preferably, from 50° C. to 125° C., more preferably, from 75° C. to 100° C., most preferably, from 80° C. to 100° C. and stirred for a period of time from 30 seconds to 12 hours, preferably, from 1 minute to 6 hours, more preferably, from 10 minutes to 4 hours, and most preferably, from 30 minutes to 3 hours.
- the first support slurry is mixed at a temperature greater than 50° C., preferably, greater than 70° C., more preferably, greater than 80° C. and most preferably, greater than 85° C., for a period of time from 30 seconds to 12 hours, preferably, from 1 minute to 6 hours, more preferably, from 10 minutes to 4 hours, and most preferably, from 30 minutes to 3 hours.
- the support slurry is mixed for a time sufficient to provide a collection of activated support particles that have the first metal catalyst compound deposited thereto.
- the first diluent can then be removed from the first support slurry to provide a dried supported first catalyst compound.
- the first diluent can be removed under vacuum or by nitrogen purge.
- a second catalyst compound is combined with the activated the first catalyst compound in the presence of a diluent comprising mineral or silicon oil in one embodiment.
- the second catalyst compound is added in a molar ratio to the first metal catalyst compound in the range from 1:1 to 3:1. Most preferably, the molar ratio is approximately 1:1.
- the resultant slurry (or first support slurry) is preferably, heated to a first temperature from 25° C. to 150° C., preferably, from 50° C. to 125° C., more preferably, from 75° C. to 100° C., most preferably, from 80° C. to 100° C. and stirred for a period of time from 30 seconds to 12 hours, preferably, from 1 minute to 6 hours, more preferably, from 10 minutes to 4 hours, and most preferably, from 30 minutes to 3 hours.
- the first diluent is an aromatic or alkane, preferably, hydrocarbon diluent having a boiling point of less than 200° C. such as toluene, xylene, hexane, etc., may be removed from the supported first metal catalyst compound under vacuum or by nitrogen purge to provide a supported mixed catalyst system. Even after addition of the oil and/or the second (or other) catalyst compound, it may be desirable to treat the slurry to further remove any remaining solvents such as toluene. This can be accomplished by an N 2 purge or vacuum, for example. Depending upon the level of mineral oil added, the resultant catalyst system may still be a slurry or may be a free flowing powder that comprises an amount of mineral oil.
- the catalyst system while a slurry of solids in mineral oil in one embodiment, may take any physical form such as a free flowing solid.
- the catalyst system may range from 1 to 99 wt % solids content by weight of the catalyst system (mineral oil, support, all catalyst compounds and activator(s)) in one embodiment.
- a polymerization process includes contacting a monomer (such as ethylene), and, optionally, comonomer (such as hexene), with a supported catalyst system comprising a group 4 (such as Hf) metallocene compound, an activator, and a support material as described above.
- a monomer such as ethylene
- comonomer such as hexene
- a supported catalyst system comprising a group 4 (such as Hf) metallocene compound, an activator, and a support material as described above.
- Monomers useful herein include substituted or unsubstituted C 2 to C 40 alpha olefins, preferably, C 2 to C 20 alpha olefins, preferably, C 2 to C 12 alpha olefins, preferably, ethylene, propylene, butene, pentene, hexene, heptene, octene, nonene, decene, undecene, dodecene and isomers thereof.
- the monomers comprise ethylene and, optional, comonomers comprising one or more C 3 to C 40 olefins, preferably, C 4 to C 20 olefins, or preferably, C 6 to C 12 olefins.
- the C 3 to C 40 olefin monomers may be linear, branched, or cyclic.
- the C 3 to C 40 cyclic olefins may be strained or unstrained, monocyclic or polycyclic, and may, optionally, include heteroatoms and/or one or more functional groups.
- Exemplary C 3 to C 40 comonomers include propylene, butene, pentene, hexene, heptene, octene, nonene, decene, undecene, dodecene, norbornene, norbornadiene, dicyclopentadiene, cyclopentene, cycloheptene, cyclooctene, cyclooctadiene, cyclododecene, 7-oxanorbornene, 7-oxanorbornadiene, substituted derivatives thereof, and isomers thereof, preferably, hexene, heptene, octene, nonene, decene, dodecene, cyclooctene, 1,5-cyclooctadiene, 1-hydroxy-4-cyclooctene, 1-acetoxy-4-cyclooctene, 5-methylcyclopentene, cyclopentene, dicyclopenta
- one or more dienes are present in the polymer produced herein at up to 10 wt %, preferably, at 0.00001 to 1.0 wt %, preferably, 0.002 to 0.5 wt %, even more preferably, 0.003 to 0.2 wt %, based upon the total weight of the composition.
- 500 ppm or less of diene is added to the polymerization, preferably, 400 ppm or less, preferably, or 300 ppm or less.
- at least 50 ppm of diene is added to the polymerization, or 100 ppm or more, or 150 ppm or more.
- Preferred diolefin monomers include any hydrocarbon structure, preferably, C 4 to C 30 , having at least two unsaturated bonds, wherein at least two of the unsaturated bonds are readily incorporated into a polymer by either a stereospecific or a non-stereospecific catalyst(s). It is further preferred that the diolefin monomers be selected from alpha, omega-diene monomers (i.e., di-vinyl monomers). More preferably, the diolefin monomers are linear di-vinyl monomers, most preferably, those containing from 4 to 30 carbon atoms.
- Examples of preferred dienes include butadiene, pentadiene, hexadiene, heptadiene, octadiene, nonadiene, decadiene, undecadiene, dodecadiene, tridecadiene, tetradecadiene, pentadecadiene, hexadecadiene, heptadecadiene, octadecadiene, nonadecadiene, icosadiene, heneicosadiene, docosadiene, tricosadiene, tetracosadiene, pentacosadiene, hexacosadiene, heptacosadiene, octacosadiene, nonacosadiene, triacontadiene, particularly preferred dienes include 1,6-heptadiene, 1,7-octadiene, 1,8-nonadiene, 1,9-decadiene
- Preferred cyclic dienes include cyclopentadiene, vinylnorbornene, norbornadiene, ethylidene norbornene, divinylbenzene, dicyclopentadiene or higher ring containing diolefins with or without substituents at various ring positions.
- a process provides polymerization of ethylene and at least one comonomer having from 3 to 8 carbon atoms, preferably, 4 to 8 carbon atoms.
- the comonomers are propylene, 1-butene, 4-methyl-1-pentene, 3-methyl-1-pentene, 1-hexene and 1-octene, the most preferred being 1-hexene, 1-butene and 1-octene.
- a process provides polymerization of one or more monomers selected from the group consisting of propylene, 1-butene, 1-pentene, 3-methyl-1-pentene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, and combinations thereof.
- Polymerization processes of the present disclosure can be carried out in any suitable manner known in the art. Any suspension, homogeneous, bulk, solution, slurry, or gas phase polymerization process known in the art can be used. Such processes can be run in a batch, semi-batch, or continuous mode. Gas phase polymerization processes and slurry processes are preferred. (A homogeneous polymerization process is a process where at least 90 wt % of the product is soluble in the reaction media.) A bulk homogeneous process is particularly preferred.
- a bulk process is a process where monomer concentration in all feeds to the reactor is 70 volume % or more.
- no solvent or diluent is present or added in the reaction medium (except for the small amounts used as the carrier for the catalyst system or other additives, or amounts typically found with the monomer; e.g., propane in propylene).
- the process is a slurry process.
- slurry polymerization process means a polymerization process where a supported catalyst is employed and monomers are polymerized on the supported catalyst particles. At least 95 wt % of polymer products derived from the supported catalyst are in granular form as solid particles (not dissolved in the diluent).
- Suitable diluents/solvents for polymerization include non-coordinating, inert liquids.
- Examples include straight and branched-chain hydrocarbons, such as isobutane, butane, pentane, isopentane, hexanes, isohexane, heptane, octane, dodecane, and mixtures thereof; cyclic and alicyclic hydrocarbons, such as cyclohexane, cycloheptane, methylcyclohexane, methylcycloheptane, and mixtures thereof, such as can be found commercially (IsoparTM); perhalogenated hydrocarbons, such as perfluorided C 4-10 alkanes, chlorobenzene, and aromatic and alkylsubstituted aromatic compounds, such as benzene, toluene, mesitylene, and xylene.
- straight and branched-chain hydrocarbons such as isobutane
- Suitable solvents also include liquid olefins, which may act as monomers or comonomers, including ethylene, propylene, 1-butene, 1-hexene, 1-pentene, 3-methyl-1-pentene, 4-methyl-1-pentene, 1-octene, 1-decene, and mixtures thereof.
- liquid olefins which may act as monomers or comonomers, including ethylene, propylene, 1-butene, 1-hexene, 1-pentene, 3-methyl-1-pentene, 4-methyl-1-pentene, 1-octene, 1-decene, and mixtures thereof.
- aliphatic hydrocarbon solvents are used as the solvent, such as isobutane, butane, pentane, isopentane, hexanes, isohexane, heptane, octane, dodecane, and mixtures thereof; cyclic and alicyclic hydrocarbons, such as cyclohexane, cycloheptane, methylcyclohexane, methylcycloheptane, and mixtures thereof.
- the solvent is not aromatic, preferably, aromatics are present in the solvent at less than 1 wt %, preferably, less than 0.5 wt %, preferably, less than 0 wt % based upon the weight of the solvents.
- a gaseous stream containing one or more monomers is continuously cycled through a fluidized bed in the presence of a catalyst under reactive conditions.
- the gaseous stream is withdrawn from the fluidized bed and recycled back into the reactor.
- polymer product is withdrawn from the reactor and fresh monomer is added to replace the polymerized monomer.
- This invention also relates to a process for the production of an ethylene alpha-olefin copolymer comprising: polymerizing ethylene and at least one alpha-olefin by contacting the ethylene and the at least one alpha-olefin with a catalyst system as described herein in at least one gas phase reactor at a reactor pressure of from 0.7 to 70 bar and a reactor temperature of from 20° C. to 150° C. to form an ethylene alpha-olefin copolymer.
- This invention also relates to an ethylene alpha-olefin copolymer obtained by contacting ethylene, at least one alpha-olefin, and a catalyst system as described herein in at least one gas-phase reactor, the copolymer having a density of 0.890 g/cc or more (ASTM D 1505), a melt flow index from 0.1 to 80 g/10 min (ASTM 1238, 190° C., 2.16 kg), and a Mw/Mn from 2 to 12.5, preferably 2.5 to 12, preferably 2 to 7.
- a slurry polymerization process generally operates between 1 to about 50 atmosphere pressure range (15 psi to 735 psi, 103 kPa to 5068 kPa) or even greater and temperatures in the range of 0° C. to about 120° C.
- a suspension of solid, particulate polymer is formed in a liquid polymerization diluent medium to which monomer and comonomers, along with catalysts, are added.
- the suspension including diluent is intermittently or continuously removed from the reactor where the volatile components are separated from the polymer and recycled, optionally after a distillation, to the reactor.
- the liquid diluent employed in the polymerization medium is typically an alkane having from 3 to 7 carbon atoms, preferably a branched alkane.
- the medium employed should be liquid under the conditions of polymerization and relatively inert. When a propane medium is used, the process must be operated above the reaction diluent critical temperature and pressure. Preferably, a hexane or an isobutane medium is employed.
- This invention also relates to a process for the production of an ethylene alpha-olefin copolymer comprising: polymerizing ethylene and at least one alpha-olefin by contacting the ethylene and the at least one alpha-olefin with a catalyst system described herein in at least one slurry phase reactor at a reactor pressure of from 0.7 to 70 bar and a reactor temperature of from 60° C. to 130° C. to form an ethylene alpha-olefin copolymer.
- This invention also relates to an ethylene alpha-olefin copolymer obtained by contacting ethylene, at least one alpha-olefin, and a catalyst system described herein in at least one slurry phase reactor, the copolymer having a density of 0.890 g/cc or more (ASTM D 1505), a melt flow index from 0.1 to 80 g/10 min (ASTM 1238, 190° C., 2.16 kg), and an Mw/Mn from 2 to 12.
- the present disclosure further provides compositions of matter produced by the methods of the present disclosure.
- the process described herein produces ethylene homopolymers or ethylene copolymers, such as ethylene-alpha-olefin (preferably C 3 to C 20 ) copolymers (such as ethylene-butene copolymers, ethylene-hexene and/or ethylene-octene copolymers).
- ethylene-alpha-olefin preferably C 3 to C 20
- copolymers such as ethylene-butene copolymers, ethylene-hexene and/or ethylene-octene copolymers.
- the copolymers produced herein have from 0 to 25 mol % (alternatively from 0.5 to 20 mol %, alternatively from 1 to 15 mol %, preferably from 3 to 10 mol %) of one or more C 3 to C 20 olefin comonomer (preferably C 3 to C 12 alpha-olefin, preferably propylene, butene, hexene, octene, decene, dodecene, preferably propylene, butene, hexene, octene).
- C 3 to C 20 olefin comonomer preferably C 3 to C 12 alpha-olefin, preferably propylene, butene, hexene, octene, decene, dodecene, preferably propylene, butene, hexene, octene.
- the monomer is ethylene and the comonomer is hexene, preferably from 1 to 15 mol % hexene, alternatively 1 to 10 mol %.
- the present disclosure provides an in-situ ethylene polymer composition having: 1) at least 50 mol % ethylene; and 2) a density of 0.89 g/cc or more, preferably 0.910 g/cc or more (ASTM 1505).
- the copolymer produced herein preferably has a composition distribution breadth T 75 -T 25 , as measured by TREF, that is greater than 20° C., preferably greater than 30° C., preferably greater than 40° C.
- the T 75 -T 25 value represents the homogeneity of the composition distribution as determined by temperature rising elution fractionation.
- a TREF curve is produced as described below.
- the temperature at which 75% of the polymer is eluted is subtracted from the temperature at which 25% of the polymer is eluted, as determined by the integration of the area under the TREF curve.
- the T 75 -T 25 value represents the difference. The closer these temperatures comes together, the narrower the composition distribution.
- the present disclosure provides an in-situ ethylene polymer composition having: 1) at least 50 mol % ethylene; and 2) a density of 0.89 g/cc or more, preferably having a density of 0.89 g/cc or more (alternately 0.90 g/cc or more, 0.908 g/cc or more, 0.91 g/cc or more, 0.918 g/cc or more, or 0.935 g/cc or more).
- the polymers produced herein have an Mw of 5,000 to 1,000,000 g/mol (preferably 25,000 to 750,000 g/mol, preferably 50,000 to 500,000 g/mol), and/or an Mw/Mn of greater than 1 to 40 (alternatively 1.5 to 20, alternatively 2 to 12, alternatively 2 to 10, alternatively 2.5 to 7) as determined by GPC-4D.
- the polymer produced herein has a unimodal or multimodal molecular weight distribution as determined by Gel Permeation Chromatography (GPC).
- GPC Gel Permeation Chromatography
- unimodal is meant that the GPC trace has one peak or two inflection points.
- multimodal is meant that the GPC trace has at least two peaks or more than 2 inflection points.
- An inflection point is that point where the second derivative of the curve changes in sign (e.g., from negative to positive or vice versa).
- the polymer produced herein has a bimodal molecular weight distribution as determined by Gel Permeation Chromatography (GPC).
- GPC Gel Permeation Chromatography
- the polymer produced herein has one, two or more peaks in the TREF measurement (see below).
- Two or more peaks in the TREF measurement as used in this specification and the appended claims is the presence of two or more distinct normalized IR response peaks in a graph of normalized IR (infrared) response (vertical or y axis) versus elution temperature (horizontal or x axis with temperature increasing from left to right) using the TREF method below.
- a “peak” in this context means where the general slope of the graph changes from positive to negative with increasing temperature. Between the two peaks is a local minimum in which the general slope of the graph changes from negative to positive with increasing temperature.
- “General trend” of the graph is intended to exclude the multiple local minimums and maximums that can occur in intervals of 2° C. or less.
- the distinct peaks are at least 3° C. apart, more preferably at least 4° C. apart, even more preferably at least 5° C. apart.
- the distinct peaks occur at a temperature on the graph above 20° C. and below 120° C. where the elution temperature is run to 0° C. or lower. This avoids confusion with the apparent peak on the graph at low temperature caused by material that remains soluble at the lowest elution temperature. Multiple peaks on such a graph indicates a multi-modal composition distribution (CD).
- Temperature Rising Elution Fractionation (TREF) analysis is done using a Crystallization Elution Fractionation (CEF) instrument from Polymer Char, S.A., Valencia, Spain.
- CEF Crystallization Elution Fractionation
- the principles of CEF analysis and a general description of the particular apparatus used are given in the article Monrabal, B. et al. Crystallization Elution Fractionation. A New Separation Process for Polyolefin Resins. Macromol. Symp. 2007, 257, 71.
- Pertinent details of the analysis method and features of the apparatus used are as follows.
- the solvent used for preparing the sample solution and for elution was 1,2-Dichlorobenzene (ODCB) which was stabilized by dissolving 1.6 g of 2,6-bis(1,1-dimethylethyl)-4-methylphenol (butylated hydroxytoluene) in a 4-L bottle of fresh solvent at ambient temperature. The stabilized solvent was then filtered using a 0.1- ⁇ m Teflon filter (Millipore). The sample (6-10 mg) to be analyzed was dissolved in 8 ml of ODCB metered at ambient temperature by stirring (Medium setting) at 150° C. for 90 min.
- ODCB 1,2-Dichlorobenzene
- a small volume of the polymer solution was first filtered by an inline filter (stainless steel, 10 ⁇ m), which is back-flushed after every filtration. The filtrate was then used to completely fill a 200- ⁇ l injection-valve loop. The volume in the loop was then introduced near the center of the CEF column (15-cm long SS tubing, 3 ⁇ 8′′ o.d., 7.8 mm i.d.) packed with an inert support (SS balls) at 140° C., and the column temperature was stabilized at 125° C. for 20 min. The sample volume was then allowed to crystallize in the column by reducing the temperature to 0° C. at a cooling rate of 1° C./min. The column was kept at 0° C.
- the distributions and the moments of molecular weight (Mw, Mn, Mw/Mn, etc.), the comonomer content (C 2 , C 3 , C 6 , etc.) and the branching index (g′vis) are determined by using a high temperature Gel Permeation Chromatography (Polymer Char GPC-IR) equipped with a multiple-channel band-filter based Infrared detector IR5, an 18-angle light scattering detector and a viscometer. Three Agilent PLgel 10- ⁇ m Mixed-B LS columns are used to provide polymer separation.
- TCB Aldrich reagent grade 1,2,4-trichlorobenzene
- BHT butylated hydroxytoluene
- the TCB mixture is filtered through a 0.1- ⁇ m Teflon filter and degassed with an online degasser before entering the GPC instrument.
- the nominal flow rate is 1.0 ml/min and the nominal injection volume is 200 ⁇ L.
- the whole system including transfer lines, columns, and detectors are contained in an oven maintained at 145° C.
- the polymer sample is weighed and sealed in a standard vial with 80- ⁇ L flow marker (Heptane) added to it.
- polymer After loading the vial in the autosampler, polymer is automatically dissolved in the instrument with 8 ml added TCB solvent. The polymer is dissolved at 160° C. with continuous shaking for about 1 hour for most PE samples or 2 hour for PP samples.
- the TCB densities used in concentration calculation are 1.463 g/ml at room temperature and 1.284 g/ml at 145° C.
- the sample solution concentration is from 0.2 to 2.0 mg/ml, with lower concentrations being used for higher molecular weight samples.
- the mass recovery is calculated from the ratio of the integrated area of the concentration chromatography over elution volume and the injection mass which is equal to the pre-determined concentration multiplied by injection loop volume.
- the conventional molecular weight (IR MW) is determined by combining universal calibration relationship with the column calibration which is performed with a series of monodispersed polystyrene (PS) standards ranging from 700 to 10M gm/mole.
- PS monodispersed polystyrene
- log ⁇ ⁇ M log ⁇ ( K PS / K ) a + 1 + a PS + 1 a + 1 ⁇ log ⁇ ⁇ M PS , where the variables with subscript “PS” stand for polystyrene while those without a subscript are for the test samples.
- ⁇ is 0.695 and K is 0.000579*(1 ⁇ 0.0087*w2b+0.000018*(w2b) ⁇ circumflex over ( ) ⁇ 2) for ethylene-butene copolymer
- w2b is a bulk weight percent of butene comonomer
- ⁇ is 0.695 and K is 0.000579*(1-0.0075*w2b) for ethylene-hexene copolymer where w2b is a bulk weight percent of hexene comonomer
- ⁇ is 0.695 and K is 0.000579*(1 ⁇ 0.0077*w2b) for ethylene-octene copolymer where w2b is a
- the comonomer composition is determined by the ratio of the IR5 detector intensity corresponding to CH 2 and CH 3 channel calibrated with a series of PE and PP homo/copolymer standards whose nominal value are predetermined by NMR or FTIR. In particular, this provides the methyls per 1000 total carbons (CH 3 /1000TC) as a function of molecular weight.
- the short-chain branch (SCB) content per 1000TC (SCB/1000TC) is then computed as a function of molecular weight by applying a chain-end correction to the CH 3 /1000TC function, assuming each chain to be linear and terminated by a methyl group at each end.
- the bulk composition of the polymer from the GPC-IR and GPC-4D analyses is obtained by considering the entire signals of the CH 3 and CH 2 channels between the integration limits of the concentration chromatogram. First, the following ratio is obtained
- the LS detector is the 18-angle Wyatt Technology High Temperature DAWN HELEOSII.
- the LS molecular weight (M) at each point in the chromatogram is determined by analyzing the LS output using the Zimm model for static light scattering ( Light Scattering from Polymer Solutions ; Huglin, M. B., Ed.; Academic Press, 1972.):
- K o ⁇ c ⁇ ⁇ ⁇ R ⁇ ( ⁇ ) 1 MP ⁇ ( ⁇ ) + 2 ⁇ A 2 ⁇ c .
- ⁇ R( ⁇ ) is the measured excess Rayleigh scattering intensity at scattering angle ⁇
- c is the polymer concentration determined from the IR5 analysis
- a 2 is the second virial coefficient
- P( ⁇ ) is the form factor for a monodisperse random coil
- K o is the optical constant for the system:
- K o 4 ⁇ ⁇ 2 ⁇ n 2 ⁇ ( dn / d ⁇ ⁇ c ) 2 ⁇ 4 ⁇ N A , where N A is Avogadro's number, and (dn/dc) is the refractive index increment for the system.
- a high temperature Agilent (or Viscotek Corporation) viscometer which has four capillaries arranged in a Wheatstone bridge configuration with two pressure transducers, is used to determine specific viscosity.
- One transducer measures the total pressure drop across the detector, and the other, positioned between the two sides of the bridge, measures a differential pressure.
- the specific viscosity, ⁇ s for the solution flowing through the viscometer is calculated from their outputs.
- the intrinsic viscosity, [ ⁇ ] ⁇ s /c, where c is concentration and is determined from the IR5 broadband channel output.
- the branching index (g′ vis ) is calculated using the output of the GPC-IR5-LS-VIS method as follows.
- the average intrinsic viscosity, [ ⁇ ] avg , of the sample is calculated by:
- the reversed-co-monomer index (RCI,m) is computed from x2 (mol % co-monomer C 3 , C 4 , C 6 , C 8 , etc.), as a function of molecular weight, where x2 is obtained from the following expression in which n is the number of carbon atoms in the comonomer (3 for C 3 , 4 for C 4 , 6 for C 6 , etc.)
- a reversed-co-monomer index (RCI,w) is also defined on the basis of the weight fraction co-monomer signal (w2/100) and is computed as follows:
- CDR-1,w, CDR-2,w, and CDR-3,w Three co-monomer distribution ratios are also defined on the basis of the % weight (w2) comonomer signal, denoted as CDR-1,w, CDR-2,w, and CDR-3,w, as follows:
- the co-monomer distribution ratios can be also defined utilizing the % mole co-monomer signal, CDR-1,m, CDR-2,m, CDR-3,m, as:
- the multi-modal polyolefin produced by the processes disclosed herein and blends thereof are useful in such forming operations as sheet and fiber extrusion and co-extrusion as well as blow molding, injection molding, and rotary molding.
- Fibers include melt spinning, solution spinning and melt blown fiber operations for use in woven or non-woven form to make filters, diaper fabrics, medical garments, geotextiles, etc.
- Extruded articles include medical tubing, wire and cable coatings, pipe, geomembranes, and pond liners. Molded articles include single and multi-layered constructions in the form of bottles, tanks, large hollow articles, rigid food containers and toys, etc.
- the polymers produced herein may be further blended with additional ethylene polymers (referred to as “second ethylene polymers” or “second ethylene copolymers”) and use in molded part and other typical polyethylene applications.
- second ethylene polymers or “second ethylene copolymers”
- the second ethylene polymer is selected from ethylene homopolymer, ethylene copolymers, and blends thereof.
- Useful second ethylene copolymers can comprise one or more comonomers in addition to ethylene and can be a random copolymer, a statistical copolymer, a block copolymer, and/or blends thereof.
- the method of making the second ethylene polymer is not critical, as it can be made by slurry, solution, gas phase, high pressure or other suitable processes, and by using catalyst systems appropriate for the polymerization of polyethylenes, such as Ziegler-Natta-type catalysts, chromium catalysts, metallocene-type catalysts, other appropriate catalyst systems or combinations thereof, or by free-radical polymerization.
- the second ethylene polymers are made by the catalysts, activators and processes described in U.S. Pat. Nos. 6,342,566; 6,384,142; 5,741,563; PCT Publication Nos. WO 03/040201; and WO 97/19991.
- Such catalysts are well known in the art, and are described in, for example, Z IEGLER C ATALYSTS (Gerhard Fink, Rolf Mülhaupt and Hans H. Brintzinger, eds., Springer-Verlag 1995); Resconi et al.; and I, II M ETALLOCENE-BASED P OLYOLEFINS (Wiley & Sons 2000). Additional useful second ethylene polymers and copolymers are described at paragraph [00118] to [00126] at pages 30 to 34 of PCT/US2016/028271, filed Apr. 19, 2016.
- This invention further relates to:
- M is a group 4 metal; each of R 1 , R 2 , R 3 , R 4 , and R 8 is independently hydrogen, halogen, C 1 -C 40 hydrocarbyl or C 1 -C 40 substituted hydrocarbyl, —NR′ 2 , —SR′, —OR, —OSiR′ 3 , —PR′ 2 , —R # —SiR′ 3 , where R # is C 1 -C 10 alkyl and each R′ is hydrogen, halogen, C 1 -C 10 alkyl, or C 6 -C 10 aryl; each of R 5 , R 5′ , R 6 , R 6′ , R 7 and R 7′ is independently hydrogen, halogen, C 1 -C 40 hydrocarbyl or C 1 -C 40 substituted hydrocarbyl, —NR′ 2 , —SR′, —OR, —OSiR′ 3 , —PR′ 2 , —R # —SiR′ 3
- M is a group 4 metal
- each of R 1 , R 2 , R 3 , R 4 , and R 8 is independently hydrogen, halogen, C 1 -C 20 substituted or unsubstituted hydrocarbyl, halocarbyl or silylcarbyl
- each of R 5 , R 5′ , R 6 , R 6′ , R 7 and R 7′ is independently hydrogen or a C 1 -C 10 alkyl
- each X is independently a leaving group, or two Xs are joined and bound to the metal atom to form a metallocycle ring, or two Xs are joined to form a chelating ligand, a diene, or an alkylidene
- each of R 9 , R 10 , R 11 , R 12 and R 13 is hydrogen or C 1 -C 20 substituted or unsubstituted hydrocarbyl, or R 9 and R 10 or R 12 and R 13 together form a substituted or unsubstit
- each of R 1 , R 2 , R 3 , and R 4 is independently halogen, C 1 -C 40 hydrocarbyl or C 1 -C 40 substituted hydrocarbyl, —NR′ 2 , —SR′, —OR, —OSiR′ 3 , —PR′ 2 , where each R′ is hydrogen, halogen, C 1 -C 10 alkyl, or C 6 -C 10 aryl.
- the catalyst is selected from:
- a catalyst system comprising: a catalyst of any of paragraphs 1 to 12; a support material; and an activator.
- the support material is selected from the group consisting of silica, alumina, silica-alumina, zirconia, and combinations thereof.
- the activator comprises alumoxane or a non-coordinating anion.
- the activator is methylalumoxane.
- the support is a silica aluminate and comprises an electron withdrawing anion such as fluoride or sulphate. 18.
- the activator is one or more of: N,N-dimethylanilinium tetrakis(perfluoronaphthyl)borate, N,N-dimethylanilinium tetrakis(perfluorobiphenyl)borate, N,N-dimethylanilinium tetrakis(perfluorophenyl)borate, N,N-dimethylanilinium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate, triphenylcarbenium tetrakis(perfluoronaphthyl)borate, triphenylcarbenium tetrakis(perfluorobiphenyl)borate, triphenylcarbenium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate, triphenylcarbenium tetrakis(perfluorophenyl)borate, [
- a process for polymerization of olefin monomers comprising contacting one or more olefin monomers with a catalyst system of any of paragraphs 13 to 21.
- 24. A process for the production of an ethylene alpha-olefin copolymer comprising: polymerizing ethylene and at least one alpha-olefin by contacting the ethylene and the at least one alpha-olefin with a catalyst system of any of paragraphs 13 to 21 in at least one gas phase reactor at a reactor pressure of from 0.7 to 70 bar and a reactor temperature of from 20° C. to 150° C.
- An ethylene alpha-olefin copolymer obtained by contacting ethylene, at least one alpha-olefin, and a catalyst system of any of paragraphs 13 to 21 in at least one gas-phase reactor, the copolymer having a density of 0.890 g/cc or more, a melt flow index from 0.1 to 80 g/10 min, and a Mw/Mn of 2 to 15. 26.
- An ethylene alpha-olefin copolymer obtained by contacting ethylene, at least one alpha-olefin selected from propylene, butene, pentene, hexene, heptene, octene, nonene, decene, undecene, and dodecene, and a catalyst system of any of paragraphs 13 to 21 in at least one gas-phase reactor, the copolymer having a density of 0.890 g/cc or more, a melt flow index from 0.1 to 80 g/10 min, and a Mw/Mn of 1.5 to 7. 27.
- a process for the production of an ethylene alpha-olefin copolymer comprising: polymerizing ethylene and at least one alpha-olefin by contacting the ethylene and the at least one alpha-olefin with a catalyst system of any of paragraphs 13 to 21 in at least one slurry phase reactor at a reactor pressure of from 0.7 to 70 bar and a reactor temperature of from 60° C. to 130° C. to form an ethylene alpha-olefin copolymer.
- ethylene homopolymerization and ethylene-hexene copolymerizations are carried out in a parallel pressure reactor, as generally described in U.S. Pat. Nos. 6,306,658; 6,455,316; PCT Publication No. WO 00/09255; and Murphy et al., J. Am. Chem. Soc., 2003, Vol. 125, pp. 4306-4317, each of which is incorporated by reference herein in its entirety.
- specific quantities, temperatures, solvents, reactants, reactants ratios, pressures, and other variables may need to be adjusted from one reaction to the next, the following describes a typical polymerization performed in a parallel, pressure reactor.
- Solvents, polymerization grade toluene and isohexane were supplied by ExxonMobil Chemical Company and thoroughly dried and degassed prior to use. Polymerization grade ethylene was used and further purified by passing it through a series of columns: 500 cc Oxyclear cylinder from Labclear (Oakland, Calif.) followed by a 500 cc column packed with dried 3 ⁇ mole sieves purchased from Aldrich Chemical Company, and a 500 cc column packed with dried 5 ⁇ mole sieves purchased from Aldrich Chemical Company.
- TnOAl tri-n-octylaluminum, neat was used as a 2 mmol/L solution in toluene.
- the autoclaves were prepared by purging with dry nitrogen prior to use.
- the transition metal compound “TMC” 100 ⁇ L of a 3 mg/mL toluene slurry, unless indicated otherwise was added via syringe with the reactor at process conditions. TnOAl was used as 200 ⁇ L of a 20 mmol/L in isohexane solution.
- Amounts of reagents not specified above are given in Table 1. Ethylene was allowed to enter (through the use of computer controlled solenoid valves) the autoclaves during polymerization to maintain reactor gauge pressure (+/ ⁇ 2 psig). Reactor temperature was monitored and typically maintained within +/ ⁇ 1° C. Polymerizations were halted by addition of approximately 50 psi O 2 /Ar (5 mol % 02) gas mixture to the autoclaves for approximately 30 seconds. The polymerizations were quenched after a predetermined cumulative amount of ethylene had been added or at a maximum of 45 minutes polymerization time. In addition to the quench time for each run, the reactors were cooled and vented. The polymer was isolated after the solvent was removed in-vacuo. Yields reported include total weight of polymer and residual catalyst. The resultant polymer was analyzed by Rapid GPC to determine the molecular weight and by DSC to determine the melting point.
- the amount of hexene incorporated in the polymers was estimated by rapid FTIR spectroscopy on a Bruker Vertex 70 IR in reflection mode. Samples were prepared in a thin film format by evaporative deposition techniques. Weight percent hexene was obtained from the ratio of peak heights in the ranges of 1377-1382 cm ⁇ 1 to 4300-4340 cm ⁇ 1 . This method was calibrated using a set of ethylene hexene copolymers with a range of known wt % hexene content.
- DSC Differential Scanning Calorimetry
- Catalyst A (n-butylCp)(2-methyl-4-phenyl-1,5,6,7- tetrahydro-s-indacenyl) ZrCl 2
- Catalyst B (Cp)(4-phenyl-1,5,6,7-tetrahydro-s- indacenyl) ZrCl 2
- Catalyst C (n-butylCp)(2-methyl-4-bromo-1,5,6,7- tetrahydro-s-indacenyl)ZrCl 2
- Catalyst D bis(2-methyl-4-phenyl-1,5,6,7-tetrahydro-s- indacenyl)ZrCl 2
- Catalyst E (n-butylCp)(4-phenyl-1,5,6,7-tetrahydro- s-indacenyl) ZrCl 2
- Catalyst F bis(4-phenyl
- CC1 is Bis (1-n-butyl-3-methyl-Cp)ZrCl 2
- CC2 is Bis(n-propylCp)HfMe 2
- CC3 is (n-butylCp)[(2-Me-4-(3′,5′-di t Bu-4′-MeO-phenyl)indenyl]ZrCl 2 .
- the residue was extracted with dichloromethane and filtered over Celite. The extract was concentrated under a stream of nitrogen and then under high vacuum. The residue was extracted with pentane. The pentane extract was concentrated under a stream of nitrogen. The pentane extract was dissolved in pentane (5 mL) and cooled to ⁇ 35° C., forming a yellow precipitate.
- a separate manifestation is as follows: To a precooled, stirring solution of iodomethane (3.476 g, 0.024 mol) in tetrahydrofuran (90 mL), a precooled solution of lithium indenide (2.389 g, 0.020 mol) in tetrahydrofuran (20 mL) was added. The reaction was stirred at room temperature for 16.5 h. Volatiles were removed under a stream of nitrogen and then under high vacuum. The residue was extracted with hexane (40 mL) and filtered over Celite. The extract was concentrated under a stream of nitrogen and then under high vacuum. The residue was extracted again with hexane (10 mL) and filtered over Celite. The extract was concentrated under a stream of nitrogen and then under high vacuum to afford a mixture of oil and solid. The oil was separated from the solid by pipette to afford the product as a clear, colorless oil (0.972 g, mixture of isomers).
- the reaction was stirred and heated to reflux for 22 h. The reaction was allowed to cool to room temperature. The reaction was quenched with hydrochloric acid (16% in water) and extracted with hexane (3 ⁇ 50 mL). The combined hexane extracts were dried with anhydrous magnesium sulfate and filtered. The dried hexane extract was concentrated under a stream of nitrogen and then under high vacuum to afford the product as a white solid (1.072 g).
- the combined diethyl ether extracts were concentrated under a stream of nitrogen and then under high vacuum. The residue was extracted with hexane. The hexane extract began to precipitate yellow solid, so the supernatant was removed, and the yellow precipitate was washed once more with hexane to afford the product as a yellow solid (0.488 g, 27%).
- Methylalumoxane treated silica prepared as follows.
- the desired amount of catalyst typically, 40 mol catalyst/g SMAO
- toluene about 3 g
- SMAO 0.5 g
- the contents of the vial were mixed (60-90 minutes) on a shaker. The contents of the vial were allowed to settle. The supernatant was decanted into solvent waste. If necessary, the remnants of each vial were stored in a freezer ( ⁇ 35° C.) until needed.
- the vials were uncapped and loaded into the sample trays in a SpeedVacTM.
- the SpeedVac was set to run at 45° C. for 45 min at 0.1 vacuum setting and run for 2-3 h. Once complete, the vials were removed, and the powder contents of each vial were poured into a separate pre-weighed 4 mL vial.
- the vials were capped, sealed with electrical tape, and stored in the dry box freezer for future use.
- Supported CC2 was made according to the general procedures described in U.S. Pat. No. 7,179,876 using (nPrCp) 2 HfMe 2 and SMAO.
- Supported CC1 was a supported catalyst made in a manner analogous to that described in U.S. Pat. No. 6,180,736 using the (1-Me-3- n BuCp) 2 ZrCl 2 metallocene and Silica 948 from Grace Davison.
- catalyst systems with unsymmetrical unbridged metallocene catalyst compounds A, B and J, featuring a combination of 4-phenyl-1,5,6,7-tetrahydro-s-indacenyl or 4-methyl-1,5,6,7-tetrahydro-s-indacenyl fragment and a Cp ligand produced polyethylene with much broader MWD than the polyethylene made from catalyst systems with comparative catalyst systems with compounds CC1 and CC2 at similar C6 wt %.
- symmetrical unbridged metallocene bis(2-Me-4-phenyl-1,5,6,7-tetrahydro-s-indacenyl)ZrCl 2 (D) and bis(4-phenyl-1,5,6,7-tetrahydro-s-indacenyl)ZrCl 2 (F) also produced polyethylene with much broader Mw/Mn in comparison to polyethylene from symmetrical unbridged metallocene CC1 and CC2. Note that under similar conditions, catalyst systems with metallocene catalyst compounds A, B, C, D, F and J showed comparable or better 1-hexene incorporation capabilities than comparative catalyst systems with compound CC1 ( FIG. 3 ).
- polymers made in Ex. 25, 28, 33, 50 and 57 have been further analyzed by GPC-4D.
- Polymers made by inventive catalysts E, F, G, and J not only have higher Mw/Mn vs. comparative catalyst CC1, but more importantly show different types of comonomer distribution than polymers from CC1 (see FIG. 4 , e.g., polymers from CC1 have similar C6 wt % at various Log M, while polymers from E, F, G and J generally show decreasing C6 wt % at increasing Log M).
- catalyst systems of the present disclosure can provide either broader (e.g., higher) Mw/Mn (for better processability), altered polymer properties (e.g. Mw, comonomer incorporation) or altered comonomer distribution.
- Catalyst systems and processes of the present disclosure could potentially provide ethylene polymers having the unique properties of good processability, high stiffness etc.
- compositions, an element or a group of elements are preceded with the transitional phrase “comprising,” it is understood that we also contemplate the same composition or group of elements with transitional phrases “consisting essentially of,” “consisting of,” “selected from the group of consisting of,” and the terms “comprising,” “consisting essentially of,” “consisting of” also include the product of the combinations of elements listed after the term.
Abstract
Description
wherein:
M is a
each of R1, R2, R3, R4, and R8 is independently hydrogen, halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl and each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl;
each of R5, R5′, R6, R6′, R7 and R7′ is independently hydrogen, halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl and each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl;
each X is independently a leaving group, or two Xs are joined and bound to the metal atom to form a metallocycle ring, or two Xs are joined to form a chelating ligand, a diene, or an alkylidene; and
each of R9, R10, R11, R12, and R13 is hydrogen, halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl and each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl, or R9 and R10 or R12 and R13 together form a substituted or unsubstituted 5-8 membered saturated or unsaturated cyclic or polycyclic ring structure.
wherein:
M is a
each of R1, R2, R3, R4, and R8 is independently hydrogen, halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl and each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl;
each of R5, R5′, R6, R6′, R7, and R7′ is independently hydrogen, halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl and each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl;
each X is independently a leaving group, or two Xs are joined and bound to the metal atom to form a metallocycle ring, or two Xs are joined to form a chelating ligand, a diene, or an alkylidene; and
each of R9, R10, R11, R12, and R13 is hydrogen, halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl and each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl, or R9 and R10 or R12 and R13 together form a substituted or unsubstituted 5-8 membered saturated or unsaturated cyclic or polycyclic ring structure.
wherein:
each of R1, R2, R3, and R4 is independently halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl and each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl. Optionally, R2 and R3 can be hydrogen, one of the R1 and R4 can be hydrogen, or R2, R3 and at least one of R1 and R4 are hydrogen.
wherein:
M is a
each of R1, R2, R3, R4, and R8 is independently hydrogen, halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl (preferably C1 to C10 alpha olefin, preferably, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, or an isomer thereof) and each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl (preferably each of R1, R2, R3, R4, and R8 is independently is H, or a C1 to C40 alpha olefin, preferably, C2 to C20 alpha olefin, preferably, C2 to C12 alpha olefin, preferably, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof);
each of R5, R5′, R6, R6′, R7, and R7′ is independently hydrogen, halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl (preferably C1 to C10 alpha olefin, preferably, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, or an isomer thereof), each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl (preferably each of R5, R5′, R6, R6′, R7, and R7′ is independently is H, or a C1 to C40 alpha olefin, preferably, C2 to C20 alpha olefin, preferably, C2 to C12 alpha olefin, preferably, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof);
each X is independently a leaving group, or two Xs are joined and bound to the metal atom to form a metallocycle ring, or two Xs are joined to form a chelating ligand, a diene, or an alkylidene (preferably each X is independently a halide, such as Cl or Br, or a C1 to C40 alpha olefin, preferably, C2 to C20 alpha olefin, preferably, C2 to C12 alpha olefin, preferably, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof); and
each of R9, R10, R11, R12, and R13 is independently hydrogen, halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl (preferably C1 to C10 alpha olefin, preferably, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, or an isomer thereof) each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl (alternately each of R9, R10, R11, R12, and R13 is independently H, C6-C10 aryl, or a C1 to C40 alpha olefin, alternately, C6-C10 aryl, C2 to C20 alpha olefin, alternately, C6-C10 aryl or C2 to C12 alpha olefin, alternately, phenyl, naphthyl, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof), or R9 and R10 or R12 and R13 together form a substituted or unsubstituted 5-8 membered saturated or unsaturated cyclic or polycyclic ring structure, such as structures represented by the formula:
wherein:
each of R1, R2, R3, and R4 is independently halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, where each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl (preferably each of R1, R2, R3, and R4, is independently H, C6-C10 aryl, or a C1 to C40 alpha olefin, preferably, C6-C10 aryl, or C2 to C20 alpha olefin, preferably, C6-C10 aryl, or C2 to C12 alpha olefin, preferably, phenyl, naphthyl, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof).
where the variables with subscript “PS” stand for polystyrene while those without a subscript are for the test samples. In this method, αPS=0.67 and KPS=0.000175 while α and K are for other materials as calculated and published in literature (Sun, T. et al. Macromolecules 2001, 34, 6812), except that for purposes of the present disclosure, α=0.695 and K=0.000579 for linear ethylene polymers, α=0.705 and K=0.0002288 for linear propylene polymers, α=0.695 and K=0.000181 for linear butene polymers, α is 0.695 and K is 0.000579*(1−0.0087*w2b+0.000018*(w2b){circumflex over ( )}2) for ethylene-butene copolymer where w2b is a bulk weight percent of butene comonomer, α is 0.695 and K is 0.000579*(1-0.0075*w2b) for ethylene-hexene copolymer where w2b is a bulk weight percent of hexene comonomer, and α is 0.695 and K is 0.000579*(1−0.0077*w2b) for ethylene-octene copolymer where w2b is a bulk weight percent of octene comonomer. Concentrations are expressed in g/cm3, molecular weight is expressed in g/mole, and intrinsic viscosity (hence K in the Mark-Houwink equation) is expressed in dL/g unless otherwise noted.
w2=f*SCB/1000TC.
The bulk composition of the polymer from the GPC-IR and GPC-4D analyses is obtained by considering the entire signals of the CH3 and CH2 channels between the integration limits of the concentration chromatogram. First, the following ratio is obtained
Then the same calibration of the CH3 and CH2 signal ratio, as mentioned previously in obtaining the CH3/1000TC as a function of molecular weight, is applied to obtain the bulk CH3/1000TC. A bulk methyl chain ends per 1000TC (bulk CH3end/1000TC) is obtained by weight-averaging the chain-end correction over the molecular-weight range. Then
w2b=f*bulk CH3/1000TC
bulk SCB/1000TC=bulk CH3/1000TC−bulk CH3end/1000TC,
and bulk SCB/1000TC is converted to bulk w2 in the same manner as described above.
Here, ΔR(θ) is the measured excess Rayleigh scattering intensity at scattering angle θ, c is the polymer concentration determined from the IR5 analysis, A2 is the second virial coefficient, P(θ) is the form factor for a monodisperse random coil, and Ko is the optical constant for the system:
where NA is Avogadro's number, and (dn/dc) is the refractive index increment for the system. The refractive index, n=1.500 for TCB at 145° C. and λ=665 nm. For analyzing polyethylene homopolymers, ethylene-hexene copolymers, and ethylene-octene copolymers, dn/dc=0.1048 ml/mg and A2=0.0015; for analyzing ethylene-butene copolymers, dn/dc=0.1048*(1-0.00126*w2) ml/mg and A2=0.0015 where w2 is weight percent butene comonomer.
where the summations are over the chromatographic slices, i, between the integration limits. The branching index g′vis is defined as
where MV is the viscosity-average molecular weight based on molecular weights determined by LS analysis and the K and a are for the reference linear polymer, which are, for purposes of the present disclosure, α=0.695 and K=0.000579 for linear ethylene polymers, α=0.705 and K=0.0002288 for linear propylene polymers, α=0.695 and K=0.000181 for linear butene polymers, α is 0.695 and K is 0.000579*(1−0.0087*w2b+0.000018*(w2b){circumflex over ( )}2) for ethylene-butene copolymer where w2b is a bulk weight percent of butene comonomer, α is 0.695 and K is 0.000579*(1−0.0075*w2b) for ethylene-hexene copolymer where w2b is a bulk weight percent of hexene comonomer, and α is 0.695 and K is 0.000579*(1−0.0077*w2b) for ethylene-octene copolymer where w2b is a bulk weight percent of octene comonomer. Concentrations are expressed in g/cm3, molecular weight is expressed in g/mole, and intrinsic viscosity (hence K in the Mark-Houwink equation) is expressed in dL/g unless otherwise noted. Calculation of the w2b values is as discussed above.
Then the molecular-weight distribution, W(z) where z=log10 M, is modified to W′(z) by setting to 0 the points in W that are less than 5% of the maximum of W; this is to effectively remove points for which the S/N in the composition signal is low. Also, points of W′ for molecular weights below 2000 gm/mole are set to 0. Then W′ is renormalized so that
1=∫−∞ ∞ W′dz,
and a modified weight-average molecular weight (Mw′) is calculated over the effectively reduced range of molecular weights as follows:
M w′=∫−∞ ∞10z *W′dz.
The RCI,m is then computed as
RCI,m=∫ −∞ ∞ x2(10z −M w′)W′dz.
A reversed-co-monomer index (RCI,w) is also defined on the basis of the weight fraction co-monomer signal (w2/100) and is computed as follows:
Note that in the above definite integrals the limits of integration are the widest possible for the sake of generality; however, in reality the function is only integrated over a finite range for which data is acquired, considering the function in the rest of the non-acquired range to be 0. Also, by the manner in which W′ is obtained, it is possible that W′ is a discontinuous function, and the above integrations need to be done piecewise.
where w2(Mw) is the % weight co-monomer signal corresponding to a molecular weight of Mw, w2(Mz) is the % weight co-monomer signal corresponding to a molecular weight of Mz, w2[(Mw+Mn)/2)] is the % weight co-monomer signal corresponding to a molecular weight of (Mw+Mn)/2, and w2[(Mz+Mw)/2] is the % weight co-monomer signal corresponding to a molecular weight of Mz+Mw/2, where Mw is the weight-average molecular weight, Mn is the number-average molecular weight, and Mz is the z-average molecular weight.
where x2(Mw) is the % mole co-monomer signal corresponding to a molecular weight of Mw, x2(Mz) is the % mole co-monomer signal corresponding to a molecular weight of Mz, x2[(Mw+Mn)/2)] is the % mole co-monomer signal corresponding to a molecular weight of (Mw+Mn)/2, and x2[(Mz+Mw)/2] is the % mole co-monomer signal corresponding to a molecular weight of Mz+Mw/2, where Mw is the weight-average molecular weight, Mn is the number-average molecular weight, and Mz is the z-average molecular weight. For purposes of the claims, GPC-4D shall be used for Mw, Mn, Mz and g′vis.
End Uses
wherein:
M is a
each of R1, R2, R3, R4, and R8 is independently hydrogen, halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl and each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl;
each of R5, R5′, R6, R6′, R7 and R7′ is independently hydrogen, halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl and each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl;
each X is independently a leaving group, or two Xs are joined and bound to the metal atom to form a metallocycle ring, or two Xs are joined to form a chelating ligand, a diene, or an alkylidene; and
each of R9, R10, R11, R12 and R13 is hydrogen, halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, —R#—SiR′3, where R# is C1-C10 alkyl and where each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl, or R9 and R10 or R12 and R13 together form a substituted or unsubstituted 5-8 membered saturated or unsaturated cyclic or multicyclic ring structure.
2. The catalyst of
M is a
each of R1, R2, R3, R4, and R8 is independently hydrogen, halogen, C1-C20 substituted or unsubstituted hydrocarbyl, halocarbyl or silylcarbyl;
each of R5, R5′, R6, R6′, R7 and R7′ is independently hydrogen or a C1-C10 alkyl;
each X is independently a leaving group, or two Xs are joined and bound to the metal atom to form a metallocycle ring, or two Xs are joined to form a chelating ligand, a diene, or an alkylidene; and
each of R9, R10, R11, R12 and R13 is hydrogen or C1-C20 substituted or unsubstituted hydrocarbyl, or R9 and R10 or R12 and R13 together form a substituted or unsubstituted 5-8 membered saturated or unsaturated cyclic ring.
3. The catalyst of
4. The catalyst of
5. The catalyst of any of
6. The catalyst of any of
7. The catalyst of any of
8. The catalyst of
9. The catalyst of any of
10. The catalyst of paragraph 1, wherein the catalyst is represented by Formula (II):
wherein:
each of R1, R2, R3, and R4 is independently halogen, C1-C40 hydrocarbyl or C1-C40 substituted hydrocarbyl, —NR′2, —SR′, —OR, —OSiR′3, —PR′2, where each R′ is hydrogen, halogen, C1-C10 alkyl, or C6-C10 aryl.
11. The catalyst of paragraph 1, wherein the catalyst is selected from:
13. A catalyst system comprising: a catalyst of any of
14. The catalyst system of paragraph 13, wherein the support material is selected from the group consisting of silica, alumina, silica-alumina, zirconia, and combinations thereof.
15. The catalyst system of
16. The catalyst system of any of
17. The catalyst system of any of paragraphs 13 to 16, wherein the support is a silica aluminate and comprises an electron withdrawing anion such as fluoride or sulphate.
18. The catalyst system of any of paragraphs 13 to 17, wherein the support is treated with an alkyl aluminum.
19. The catalyst system of any of paragraphs 13 to 18, wherein the catalyst represented by formula (I) is present in the catalyst system as at least two isomers.
20. The catalyst system of any of paragraphs 13 to 19 wherein the support is silica.
21. The catalyst system of any of paragraphs 13 to 20, wherein the activator is one or more of: N,N-dimethylanilinium tetrakis(perfluoronaphthyl)borate, N,N-dimethylanilinium tetrakis(perfluorobiphenyl)borate, N,N-dimethylanilinium tetrakis(perfluorophenyl)borate, N,N-dimethylanilinium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate, triphenylcarbenium tetrakis(perfluoronaphthyl)borate, triphenylcarbenium tetrakis(perfluorobiphenyl)borate, triphenylcarbenium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate, triphenylcarbenium tetrakis(perfluorophenyl)borate, [Me3NH+][B(C6F5)4 −], 1-(4-(tris(pentafluorophenyl)borate)-2,3,5,6-tetrafluorophenyl) pyrrolidinium, 1-(4-(tris(pentafluorophenyl)borate)-2,3,5,6-tetrafluorophenyl) pyrrolidinium, sodium tetrakis(pentafluorophenyl)borate, potassium tetrakis(pentafluorophenyl)borate, 4-(tris(pentafluorophenyl)borate)-2,3,5,6-tetrafluoropyridinium, sodium tetrakis(perfluorophenyl)aluminate, potassium terakis(pentafluorophenyl), and N,N-dimethylanilinium tetrakis(perfluorophenyl)aluminate.
22. A process for polymerization of olefin monomers comprising contacting one or more olefin monomers with a catalyst system of any of paragraphs 13 to 21.
23. The process of paragraph 22, wherein polymerization of the olefin monomers forms linear low density polyethylene.
24. A process for the production of an ethylene alpha-olefin copolymer comprising: polymerizing ethylene and at least one alpha-olefin by contacting the ethylene and the at least one alpha-olefin with a catalyst system of any of paragraphs 13 to 21 in at least one gas phase reactor at a reactor pressure of from 0.7 to 70 bar and a reactor temperature of from 20° C. to 150° C. to form an ethylene alpha-olefin copolymer.
25. An ethylene alpha-olefin copolymer obtained by contacting ethylene, at least one alpha-olefin, and a catalyst system of any of paragraphs 13 to 21 in at least one gas-phase reactor, the copolymer having a density of 0.890 g/cc or more, a melt flow index from 0.1 to 80 g/10 min, and a Mw/Mn of 2 to 15.
26. An ethylene alpha-olefin copolymer obtained by contacting ethylene, at least one alpha-olefin selected from propylene, butene, pentene, hexene, heptene, octene, nonene, decene, undecene, and dodecene, and a catalyst system of any of paragraphs 13 to 21 in at least one gas-phase reactor, the copolymer having a density of 0.890 g/cc or more, a melt flow index from 0.1 to 80 g/10 min, and a Mw/Mn of 1.5 to 7.
27. The copolymer of any of paragraphs 25 to 26, wherein the copolymer has an Mw value of 50,000 to 1,000,000 g/mol.
28. A process for the production of an ethylene alpha-olefin copolymer comprising: polymerizing ethylene and at least one alpha-olefin by contacting the ethylene and the at least one alpha-olefin with a catalyst system of any of paragraphs 13 to 21 in at least one slurry phase reactor at a reactor pressure of from 0.7 to 70 bar and a reactor temperature of from 60° C. to 130° C. to form an ethylene alpha-olefin copolymer.
29. An ethylene alpha-olefin copolymer obtained by contacting ethylene, at least one alpha-olefin, and a catalyst system of any of paragraphs 13 to 21 in at least one slurry phase reactor, the copolymer having a density of 0.890 g/cc or more, a melt flow index from 0.1 to 80 g/10 min, and an Mw/Mn from 2 to 12.
30. The catalyst of paragraph 11, wherein R2 and R3 are hydrogen, one of the R1 and R4 are hydrogen, or R2, R3 and at least one of R1 and R4 are hydrogen.
Experimental
General Procedure for High Throughput Ethylene/1-hexene Polymerization and Polymer Characterization (Table 1)
Catalyst A |
(n-butylCp)(2-methyl-4-phenyl-1,5,6,7- |
tetrahydro-s-indacenyl) ZrCl2 |
|
Catalyst B |
(Cp)(4-phenyl-1,5,6,7-tetrahydro-s- |
indacenyl) ZrCl2 |
|
Catalyst C |
(n-butylCp)(2-methyl-4-bromo-1,5,6,7- |
tetrahydro-s-indacenyl)ZrCl2 |
|
Catalyst D |
bis(2-methyl-4-phenyl-1,5,6,7-tetrahydro-s- |
indacenyl)ZrCl2 |
|
Catalyst E |
(n-butylCp)(4-phenyl-1,5,6,7-tetrahydro- |
s-indacenyl) ZrCl2 |
|
Catalyst F |
bis(4-phenyl-1,5,6,7-tetrahydro-s- |
indacenyl)ZrCl2 |
|
Catalyst G |
(1-butyl-3-methyl-Cp)(4-phenyl-1,5,6,7- |
tetrahydro-s-indacenyl) ZrCl2 |
|
Catalyst H |
(1-butyl-3-phenyl-Cp)(2-methyl-4-bromo- |
1,5,6,7-tetrahydro-s-indacenyl) ZrCl2 |
|
Catalyst I |
(1-Methyl-Ind)(2-methyl-4-bromo- |
1,5,6,7-tetrahydro-s-indacenyl) ZrCl2 |
|
Catalyst J |
(n-ButylCp)(2,4-dimethyl-1,5,6,7- |
tetrahydro-s-indacenyl)ZrCl2 |
Comparative Catalyst Compounds:
TABLE 1 |
High Throughput Ethylene Polymerization and Ethylene 1-Hexene Copolymerization Using |
Supported Catalysts. Conditions: 0.3 mg supported catalysts, isohexane solvent, total volume = |
5 mL. Polymerization temperature (Tp) = 85° C., 130 psi ethylene. |
Mw | Mn | Mw/Mn | Activity | ||||||||
C6 | C6 | (Rapid | (Rapid | (Rapid | Tm | time | yield | (g pol/g | C6 wt % | ||
Ex | Cat | (μL) | wt % | GPC) | GPC) | GPC) | (° C.) | (s) | (g) | cat. h) | (average) |
1 | A | 0 | 0.0 | 426622 | 163455 | 2.6 | 136.2 | 2352 | 0.0799 | 408 | |
2 | A | 60 | 2.2 | 423311 | 111597 | 3.8 | 126.2 | 2701 | 0.0557 | 248 | 2.1 |
3 | A | 60 | 2.1 | 404009 | 100176 | 4.0 | 126.1 | 2626 | 0.0592 | 271 | |
4 | A | 180 | 6.9 | 384674 | 74611 | 5.2 | 121.0 | 2700 | 0.0572 | 255 | 7.0 |
5 | A | 180 | 7.2 | 369674 | 86529 | 4.3 | 121.0 | 2700 | 0.058 | 258 | |
6 | A | 240 | 8.5 | 336660 | 64160 | 5.2 | 120.2 | 2700 | 0.0462 | 206 | |
7 | B | 0 | 0.0 | 687732 | 236999 | 2.9 | 135.4 | 2700 | 0.0377 | 168 | |
8 | B | 60 | 2.6 | 465078 | 134933 | 3.4 | 124.9 | 2701 | 0.0382 | 170 | 3.1 |
9 | B | 60 | 3.7 | 453757 | 142610 | 3.2 | 124.6 | 1567 | 0.0346 | 266 | |
10 | B | 180 | 8.1 | 358407 | 83817 | 4.3 | 119.8 | 2701 | 0.0375 | 167 | 8.2 |
11 | B | 180 | 8.3 | 332710 | 83717 | 4.0 | 119.3 | 2701 | 0.0568 | 253 | |
12 | B | 240 | 7.1 | 344106 | 103126 | 3.3 | 119.7 | 373 | 0.0117 | 377 | |
13 | C | 0 | 0.0 | 583344 | 224821 | 2.6 | 136.0 | 2217 | 0.0769 | 417 | |
14 | C | 60 | 1.3 | 445546 | 182727 | 2.4 | 124.8 | 1107 | 0.0893 | 970 | 1.2 |
15 | C | 60 | 1.2 | 479329 | 227249 | 2.1 | 125.3 | 1302 | 0.0925 | 854 | |
16 | C | 180 | 5.4 | 482654 | 196787 | 2.5 | 118.6 | 812 | 0.0915 | 1355 | |
17 | D | 0 | 0.0 | 968511 | 312564 | 3.1 | 136.0 | 2700 | 0.0297 | 132 | |
18 | D | 60 | 1.2 | 564983 | 117777 | 4.8 | 128.9 | 2700 | 0.0189 | 84 | 1.4 |
19 | D | 60 | 1.5 | 487107 | 95000 | 5.1 | 129.0 | 2700 | 0.0147 | 65 | |
20 | D | 180 | 5.1 | 287901 | 54249 | 5.3 | 125.6 | 2701 | 0.0133 | 59 | 4.9 |
21 | D | 180 | 4.7 | 302986 | 43449 | 7.0 | 125.9 | 2700 | 0.0124 | 55 | |
22 | D | 240 | 8.0 | 226490 | 45617 | 5.0 | 124.8 | 2701 | 0.0128 | 57 | |
23 | E | 60 | 1.1 | 299064 | 128491 | 2.3 | 126.4 | 905 | 0.0942 | 1252 | |
24 | E | 180 | 4.3 | 241971 | 105803 | 2.3 | 121.0 | 604 | 0.0842 | 1675 | |
25 | E | 240 | 5.7 | 264409 | 111304 | 2.4 | 119.9 | 621 | 0.0904 | 1749 | |
26 | F | 0 | 0.0 | 428516 | 167606 | 2.6 | 135.4 | 1344 | 0.0505 | 452 | |
27 | F | 60 | 3.9 | 185128 | 64554 | 2.9 | 124.6 | 1084 | 0.0953 | 1057 | |
28 | F | 180 | 10.8 | 110594 | 29869 | 3.7 | 123.9 | 1008 | 0.1001 | 1194 | |
29 | F | 360 | 16.4 | 86061 | 19557 | 4.4 | 123.3 | 1906 | 0.1034 | 652 | |
30 | G | 0 | 0.0 | 417814 | 176183 | 2.4 | 135.6 | 1775 | 0.093 | 630 | |
31 | G | 60 | 1.2 | 263121 | 112249 | 2.3 | 127.4 | 1003 | 0.0926 | 1111 | |
32 | G | 180 | 3.9 | 218262 | 95571 | 2.3 | 122.3 | 572 | 0.0915 | 1922 | |
33 | G | 240 | 7.4 | 214764 | 95499 | 2.2 | 121.0 | 648 | 0.0946 | 1756 | |
34 | G | 300 | 6.8 | 220701 | 87682 | 2.5 | 120.2 | 712 | 0.0964 | 1628 | |
35 | G | 360 | 7.0 | 213721 | 76312 | 2.8 | 118.7 | 808 | 0.0929 | 1382 | |
36 | H | 0 | 0.0 | 589888 | 251618 | 2.3 | 135.0 | 2700 | 0.0607 | 270 | |
37 | H | 60 | 1.7 | 568097 | 276972 | 2.1 | 125.3 | 2125 | 0.0909 | 514 | |
38 | H | 60 | 1.7 | 550956 | 250382 | 2.2 | 123.9 | 1481 | 0.072 | 585 | |
39 | H | 180 | 4.4 | 503492 | 204440 | 2.5 | 118.2 | 1541 | 0.0884 | 690 | |
40 | H | 180 | 3.7 | 525829 | 178466 | 2.9 | 117.6 | 1443 | 0.0958 | 799 | |
41 | H | 240 | 5.8 | 498614 | 156738 | 3.2 | 116.1 | 2312 | 0.1026 | 534 | |
42 | I | 0 | 0.0 | 420289 | 195580 | 2.1 | 135.5 | 2701 | 0.0534 | 238 | |
43 | I | 60 | 0.5 | 383019 | 192493 | 2.0 | 128.6 | 2660 | 0.0755 | 341 | |
44 | I | 60 | 0.8 | 376204 | 188895 | 2.0 | 128.9 | 2701 | 0.0782 | 348 | |
45 | I | 180 | 3.1 | 358830 | 151378 | 2.4 | 124.3 | 2702 | 0.0812 | 361 | |
46 | I | 180 | 3.6 | 357563 | 144073 | 2.5 | 123.3 | 2700 | 0.0842 | 375 | |
47 | I | 240 | 4.6 | 329911 | 122096 | 2.7 | 122.2 | 2701 | 0.0832 | 370 | |
48 | J | 0 | 0.0 | 615164 | 207577 | 3.0 | 135.9 | 2701 | 0.0796 | 354 | |
49 | J | 60 | 3.5 | 491589 | 145723 | 3.4 | 126.3 | 2275 | 0.0907 | 479 | |
50 | J | 180 | 7.7 | 376094 | 77214 | 4.9 | 121.3 | 1649 | 0.0555 | 405 | |
51 | CC1 | 0 | 0.0 | 595381 | 264421 | 2.3 | 136.4 | 2498 | 0.0887 | 427 | |
52 | CC1 | 60 | 2.1 | 482338 | 223939 | 2.2 | 125.4 | 1386 | 0.0928 | 805 | 2.2 |
53 | CC1 | 60 | 2.4 | 462870 | 218017 | 2.1 | 125.6 | 1332 | 0.0905 | 817 | |
54 | CC1 | 180 | 5.6 | 505142 | 252255 | 2.0 | 117.9 | 1001 | 0.0963 | 1157 | 5.6 |
55 | CC1 | 180 | 5.7 | 546395 | 289367 | 1.9 | 117.9 | 927 | 0.0975 | 1265 | |
56 | CC1 | 240 | 6.8 | 588707 | 305332 | 1.9 | 115.8 | 871 | 0.0961 | 1327 | 6.5 |
57 | CC1 | 240 | 6.1 | 533791 | 288487 | 1.9 | 114.6 | 803 | 0.0995 | 1489 | |
58 | CC2 | 0 | 0.0 | 1353958 | 659383 | 2.1 | 136.5 | 532 | 0.0948 | 2144 | 0.0 |
59 | CC2 | 60 | 4.2 | 1231134 | 535748 | 2.3 | 120.0 | 605 | 0.0986 | 1960 | 4.1 |
60 | CC2 | 60 | 4.1 | 1266190 | 609847 | 2.1 | 120.0 | 604 | 0.0906 | 1805 | |
61 | CC2 | 180 | 9.9 | 1657034 | 732820 | 2.3 | 108.6 | 1165 | 0.0961 | 992 | 9.7 |
62 | CC2 | 180 | 9.5 | 1748845 | 752980 | 2.3 | 108.8 | 922 | 0.098 | 1279 | |
63 | CC2 | 240 | 11.9 | 1681855 | 768666 | 2.2 | 109.2 | 2701 | 0.0749 | 333 | |
64 | CC3 | 0 | 0.0 | 490897 | 244083 | 2.0 | 135.4 | 2700 | 0.0683 | 304 | 0.0 |
65 | CC3 | 60 | 2.8 | 413364 | 176824 | 2.3 | 123.9 | 1076 | 0.0861 | 962 | 2.9 |
66 | CC3 | 60 | 3.0 | 410065 | 198910 | 2.1 | 124.2 | 1243 | 0.0905 | 875 | |
67 | CC3 | 180 | 5.2 | 434486 | 206429 | 2.1 | 117.4 | 927 | 0.0945 | 1226 | |
C6 | Mw (GPC-4D) | |||
Ex. | Cat. | (μL) | kg/mol | Mw/Mn (GPC-4D) |
25 | |
240 | 114 | 3.3 |
28 | |
180 | 37 | 3.5 |
33 | |
240 | 98 | 3.2 |
50 | |
180 | 158 | 6.7 |
57 | |
240 | 226 | 2.7 |
Claims (30)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16/153,256 US11001657B2 (en) | 2017-10-25 | 2018-10-05 | Unbridged indacenyl metallocenes |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201762577046P | 2017-10-25 | 2017-10-25 | |
US16/153,256 US11001657B2 (en) | 2017-10-25 | 2018-10-05 | Unbridged indacenyl metallocenes |
Publications (2)
Publication Number | Publication Date |
---|---|
US20190119418A1 US20190119418A1 (en) | 2019-04-25 |
US11001657B2 true US11001657B2 (en) | 2021-05-11 |
Family
ID=66170975
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US16/153,256 Active 2039-01-01 US11001657B2 (en) | 2017-10-25 | 2018-10-05 | Unbridged indacenyl metallocenes |
Country Status (1)
Country | Link |
---|---|
US (1) | US11001657B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11345766B2 (en) * | 2016-05-03 | 2022-05-31 | Exxonmobil Chemical Patents Inc. | Tetrahydro-as-indacenyl catalyst composition, catalyst system, and processes for use thereof |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11059918B2 (en) | 2016-05-27 | 2021-07-13 | Exxonmobil Chemical Patents Inc. | Metallocene catalyst compositions and polymerization process therewith |
JP7329256B2 (en) * | 2018-02-07 | 2023-08-18 | ユーピー ケミカル カンパニー リミテッド | Group 4 metal element-containing compound, method for producing the same, film-forming precursor composition containing the same, and method for forming a film using the same |
CN111868106B (en) | 2018-02-12 | 2023-02-17 | 埃克森美孚化学专利公司 | Catalyst system and process for poly-alpha-olefins having high vinylidene content |
US11472828B2 (en) | 2019-10-11 | 2022-10-18 | Exxonmobil Chemical Patents Inc. | Indacene based metallocene catalysts useful in the production of propylene polymers |
CN115485311A (en) | 2020-02-24 | 2022-12-16 | 埃克森美孚化学专利公司 | Ansa-bis (inden-2-yl) catalysts for the production of vinylidene-terminated polyalphaolefins |
WO2021188361A1 (en) | 2020-03-20 | 2021-09-23 | Exxonmobil Chemical Patents Inc. | Linear alpha-olefin copolymers and impact copolymers thereof |
US11766669B2 (en) | 2020-06-26 | 2023-09-26 | Exxonmobil Chemical Patents Inc. | Hexahydrocyclopenta[e]-as-indacen-1-yl and octahydrobenzo[e]-as-indacen-1-yl based catalyst complexes and process for use thereof |
WO2022108973A1 (en) | 2020-11-23 | 2022-05-27 | Exxonmobil Chemical Patents Inc. | Metallocene polypropylene prepared using aromatic solvent-free supports |
WO2023034889A1 (en) | 2021-09-02 | 2023-03-09 | Exxonmobil Chemical Patents Inc. | C1 symmetric metallocene catalysts tailored for production of vinyl-terminated polypropylene oligomers and macromonomers |
Citations (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060024520A1 (en) | 2004-08-02 | 2006-02-02 | Dan-Cheng Kong | Permeable polypropylene film |
US20060024518A1 (en) | 2004-08-02 | 2006-02-02 | Dan-Cheng Kong | Low density cavitated opaque polymer film |
US20070276110A1 (en) | 2006-05-23 | 2007-11-29 | Dow Global Technologies Inc. | High-density polyethylene compositions and method of making the same |
US7452949B2 (en) | 2003-12-10 | 2008-11-18 | Basell Polyolefine Gmbh | Organometallic transition metal compound, biscyclopentadienyl ligand system, catalyst system and preparation of polyolefins |
US7601666B2 (en) | 2004-07-08 | 2009-10-13 | Exxonmobil Chemical Patents Inc. | Olefin polymerization catalyst system and process for use thereof |
US7842764B2 (en) | 2005-03-18 | 2010-11-30 | Basell Poliolefine Italia S.R.L. | Metallocene compounds |
WO2011012245A1 (en) | 2009-07-27 | 2011-02-03 | Basell Polyolefine Gmbh | Organometallic transition metal compound, catalyst system and preparation of polyolefins |
US8785575B2 (en) | 2006-04-21 | 2014-07-22 | Basell Polyolefine Gmbh | Process for the preparation of ethylene propylene copolymers |
US8809563B2 (en) | 2009-11-09 | 2014-08-19 | Exxonmobil Chemical Patents Inc. | Metathesis catalyst and process for use thereof |
US20150284489A1 (en) | 2014-04-03 | 2015-10-08 | Equistar Chemicals, Lp | Non-bridged metallocene complexes for the polymerization of olefins |
US20150284490A1 (en) | 2014-04-03 | 2015-10-08 | Equistar Chemicals, Lp | Substituted zirconocenes catalysts and methods of use in polymerization reactions |
US20150322184A1 (en) | 2014-05-07 | 2015-11-12 | Chevron Phillips Chemical Company Lp | High Performance Moisture Barrier Films at Lower Densities |
US9266910B2 (en) | 2013-10-29 | 2016-02-23 | Exxonmobil Chemical Patents Inc. | Asymmetric polypropylene catalysts |
US9458254B2 (en) | 2013-07-17 | 2016-10-04 | Exxonmobil Chemical Patents Inc. | Substituted metallocene catalysts |
WO2016196331A1 (en) | 2015-06-05 | 2016-12-08 | Exxonmobil Chemical Patents Inc. | Supported metallocene catalyst systems for polymerization |
US9796795B2 (en) | 2015-01-14 | 2017-10-24 | Exxonmobil Chemical Patents Inc. | Tetrahydroindacenyl catalyst composition, catalyst system, and processes for use thereof |
US9803037B1 (en) | 2016-05-03 | 2017-10-31 | Exxonmobil Chemical Patents Inc. | Tetrahydro-as-indacenyl catalyst composition, catalyst system, and processes for use thereof |
WO2017204830A1 (en) | 2016-05-27 | 2017-11-30 | Exxonmobil Chemical Patents, Inc. | Metallocene catalyst compositions and polymerization process therewith |
US20180094088A1 (en) | 2016-10-05 | 2018-04-05 | Exxonmobil Chemical Patents Inc. | Sterically Hindered Metallocenes, Synthesis and Use |
US9938364B2 (en) | 2013-07-17 | 2018-04-10 | Exxonmobil Chemical Patents Inc. | Substituted metallocene catalysts |
US20190144571A1 (en) | 2017-11-14 | 2019-05-16 | Exxonmobil Chemical Patents Inc. | (Di)Silicon Bridged Metallocenes that Produce Polyethylene with Broad Molecular Weight Distribution and High Molecular Weight |
US20190161560A1 (en) | 2017-11-29 | 2019-05-30 | Exxonmobil Chemical Patents Inc. | Asymmetric ANSA-Metallocene Catalyst Compounds for Producing Polyolefins Having a Broad Molecular Weight Distribution |
US20190263953A1 (en) | 2017-11-14 | 2019-08-29 | Exxonmobil Chemical Patents Inc. | Polyethylene Compositions and Articles Made Therefrom |
US20190284311A1 (en) | 2018-03-19 | 2019-09-19 | Exxonmobil Chemical Patents Inc. | Processes for Producing High Propylene Content PEDM Using Tetrahydroindacenyl Catalyst Systems |
-
2018
- 2018-10-05 US US16/153,256 patent/US11001657B2/en active Active
Patent Citations (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7452949B2 (en) | 2003-12-10 | 2008-11-18 | Basell Polyolefine Gmbh | Organometallic transition metal compound, biscyclopentadienyl ligand system, catalyst system and preparation of polyolefins |
US7601666B2 (en) | 2004-07-08 | 2009-10-13 | Exxonmobil Chemical Patents Inc. | Olefin polymerization catalyst system and process for use thereof |
US20060024520A1 (en) | 2004-08-02 | 2006-02-02 | Dan-Cheng Kong | Permeable polypropylene film |
US20060024518A1 (en) | 2004-08-02 | 2006-02-02 | Dan-Cheng Kong | Low density cavitated opaque polymer film |
US7842764B2 (en) | 2005-03-18 | 2010-11-30 | Basell Poliolefine Italia S.R.L. | Metallocene compounds |
US8785575B2 (en) | 2006-04-21 | 2014-07-22 | Basell Polyolefine Gmbh | Process for the preparation of ethylene propylene copolymers |
US20070276110A1 (en) | 2006-05-23 | 2007-11-29 | Dow Global Technologies Inc. | High-density polyethylene compositions and method of making the same |
WO2011012245A1 (en) | 2009-07-27 | 2011-02-03 | Basell Polyolefine Gmbh | Organometallic transition metal compound, catalyst system and preparation of polyolefins |
US8809563B2 (en) | 2009-11-09 | 2014-08-19 | Exxonmobil Chemical Patents Inc. | Metathesis catalyst and process for use thereof |
US9938364B2 (en) | 2013-07-17 | 2018-04-10 | Exxonmobil Chemical Patents Inc. | Substituted metallocene catalysts |
US9458254B2 (en) | 2013-07-17 | 2016-10-04 | Exxonmobil Chemical Patents Inc. | Substituted metallocene catalysts |
US9266910B2 (en) | 2013-10-29 | 2016-02-23 | Exxonmobil Chemical Patents Inc. | Asymmetric polypropylene catalysts |
US20150284490A1 (en) | 2014-04-03 | 2015-10-08 | Equistar Chemicals, Lp | Substituted zirconocenes catalysts and methods of use in polymerization reactions |
US20150284489A1 (en) | 2014-04-03 | 2015-10-08 | Equistar Chemicals, Lp | Non-bridged metallocene complexes for the polymerization of olefins |
US20150322184A1 (en) | 2014-05-07 | 2015-11-12 | Chevron Phillips Chemical Company Lp | High Performance Moisture Barrier Films at Lower Densities |
US9796795B2 (en) | 2015-01-14 | 2017-10-24 | Exxonmobil Chemical Patents Inc. | Tetrahydroindacenyl catalyst composition, catalyst system, and processes for use thereof |
WO2016196331A1 (en) | 2015-06-05 | 2016-12-08 | Exxonmobil Chemical Patents Inc. | Supported metallocene catalyst systems for polymerization |
US9803037B1 (en) | 2016-05-03 | 2017-10-31 | Exxonmobil Chemical Patents Inc. | Tetrahydro-as-indacenyl catalyst composition, catalyst system, and processes for use thereof |
US10280240B2 (en) | 2016-05-27 | 2019-05-07 | Exxonmobil Chemical Patents Inc. | Metallocene catalyst compositions and polymerization process therewith |
WO2017204830A1 (en) | 2016-05-27 | 2017-11-30 | Exxonmobil Chemical Patents, Inc. | Metallocene catalyst compositions and polymerization process therewith |
US20180094088A1 (en) | 2016-10-05 | 2018-04-05 | Exxonmobil Chemical Patents Inc. | Sterically Hindered Metallocenes, Synthesis and Use |
US20190144571A1 (en) | 2017-11-14 | 2019-05-16 | Exxonmobil Chemical Patents Inc. | (Di)Silicon Bridged Metallocenes that Produce Polyethylene with Broad Molecular Weight Distribution and High Molecular Weight |
US20190263953A1 (en) | 2017-11-14 | 2019-08-29 | Exxonmobil Chemical Patents Inc. | Polyethylene Compositions and Articles Made Therefrom |
US20190161560A1 (en) | 2017-11-29 | 2019-05-30 | Exxonmobil Chemical Patents Inc. | Asymmetric ANSA-Metallocene Catalyst Compounds for Producing Polyolefins Having a Broad Molecular Weight Distribution |
US20190284311A1 (en) | 2018-03-19 | 2019-09-19 | Exxonmobil Chemical Patents Inc. | Processes for Producing High Propylene Content PEDM Using Tetrahydroindacenyl Catalyst Systems |
US20190284318A1 (en) | 2018-03-19 | 2019-09-19 | Exxonmobil Chemical Patents Inc. | Processes for Producing High Propylene Content PEDM Having Low Glass Transition Temperatures Using Tetrahydroindacenyl Catalyst Systems |
Non-Patent Citations (11)
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11345766B2 (en) * | 2016-05-03 | 2022-05-31 | Exxonmobil Chemical Patents Inc. | Tetrahydro-as-indacenyl catalyst composition, catalyst system, and processes for use thereof |
Also Published As
Publication number | Publication date |
---|---|
US20190119418A1 (en) | 2019-04-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US11001657B2 (en) | Unbridged indacenyl metallocenes | |
US10913808B2 (en) | Mixed catalysts with unbridged hafnocenes with -CH2-SiMe3 moieties | |
US10730038B2 (en) | Metallocene catalysts, catalyst systems, and methods for using the same | |
US10723819B2 (en) | Supported catalyst systems and processes for use thereof | |
US11161922B2 (en) | Toluene free silica supported single-site metallocene catalysts from in-situ supported MAO formation in aliphatic solvents | |
US10479846B2 (en) | Hafnocene catalyst compounds and process for use thereof | |
US11274196B2 (en) | Polyethylene compositions and films prepared therefrom | |
US20200048382A1 (en) | Mixed Catalyst Systems and Methods of Using the Same | |
US11021552B2 (en) | Toluene free silica supported single-site metallocene catalysts from in-situ supported alumoxane formation in aliphatic solvents | |
US11712687B2 (en) | Catalyst systems and polymerization processes for using the same | |
US10703838B2 (en) | Mixed catalyst systems with four metallocenes on a single support | |
US9988410B2 (en) | Substituted bis indenyl metallocene catalyst compounds comprising-Si—Si-bridge | |
US10844150B2 (en) | Mixed catalysts with 2,6-bis(imino)pyridyl iron complexes and bridged hafnocenes | |
US20190248929A1 (en) | Benzindenyl Catalyst Systems and Processes for Use Thereof | |
US10926250B2 (en) | Catalyst systems and polymerization processes for using the same | |
US11198747B2 (en) | Catalyst systems including two hafnocene catalyst compounds | |
US20210016265A1 (en) | Mixed Catalyst System | |
EP3583140B1 (en) | Supported catalyst systems and processes for use thereof | |
US10954328B2 (en) | Polymerization processes | |
EP3661975B1 (en) | Mixed catalysts with 2, 6-bis(imino)pyridyl iron complexes and bridged hafnocenes | |
WO2019083709A1 (en) | Unbridged indacenyl metallocenes | |
WO2019157162A1 (en) | Benzindenyl catalyst systems and processes for use thereof | |
EP3802643A1 (en) | Catalyst systems including two hafnocene catalyst compounds | |
WO2019027586A1 (en) | Mixed catalysts with 2, 6-bis(imino)pyridy| iron complexes and bridged hafnocenes |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FEPP | Fee payment procedure |
Free format text: ENTITY STATUS SET TO UNDISCOUNTED (ORIGINAL EVENT CODE: BIG.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
AS | Assignment |
Owner name: EXXONMOBIL CHEMICAL PATENTS INC., TEXAS Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:YANG, JIAN;KARAHALIS, GREGORY;REEL/FRAME:047682/0342 Effective date: 20181113 |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: NON FINAL ACTION MAILED |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: NOTICE OF ALLOWANCE MAILED -- APPLICATION RECEIVED IN OFFICE OF PUBLICATIONS |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: PUBLICATIONS -- ISSUE FEE PAYMENT RECEIVED |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: PUBLICATIONS -- ISSUE FEE PAYMENT VERIFIED |
|
STCF | Information on status: patent grant |
Free format text: PATENTED CASE |